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Nova Eye Medical Limited

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Year Founded & Workforce

1985

50 Employees

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Nova Eye Medical Limited Overview

Nova Eye Medical is a small-cap Australian–American ophthalmic medtech company built around one core franchise: iTrack™ canaloplasty. It is a single-use, catheter-based minimally invasive glaucoma surgery (MIGS) that viscodilates Schlemm's canal through 360 degrees and restores the eye's natural outflow pathway without leaving a stent or removing tissue. The company emerged in July 2020 when Ellex Medical Lasers sold its capital-equipment laser and ultrasound business to France's Lumibird for A$100 million. The remaining entity kept the consumables franchise, the Molteno3® glaucoma drainage device acquired in New Zealand, and the 2RT® retinal laser (housed in the AlphaRET subsidiary). Since the US launch of iTrack™ Advance in 2023, revenue has compounded at more than 25% a year for four consecutive years, reaching A$34.9 million (US$23.7 million) in FY2026. The group recorded its first EBITDA-positive half in H2 FY2026. It is a sub-scale challenger to Glaukos, Alcon and Sight Sciences in a roughly US$944 million interventional glaucoma market, with about 3–5% procedure share in its core US segment.


Company's own description

In its standard ASX boilerplate (2025–2026), Nova Eye describes itself as a medical technology company that develops, manufactures and sells a portfolio of proprietary ophthalmic treatment technologies and devices used by eye surgeons globally. Those technologies are the iTrack™ consumable glaucoma surgical device, which restores the eye's natural outflow pathway to lower intraocular pressure (IOP) and reduce patient reliance on anti-glaucoma medications in mild-to-moderate glaucoma, and the Molteno3® glaucoma drainage device platform for severe glaucoma. Its sales headquarters is in Fremont, California, supported by a global network of distribution partners, and manufacturing is in Fremont and Dunedin, New Zealand (ASX releases 26 Feb 2026, 5 May 2026; InvestSMART company profile).

The FY2025 and FY2026 Annual Reports describe two operating segments:

Glaucoma Surgical Devices: design, manufacture, marketing and sale of iTrack, iTrack Advance and Molteno3.

AlphaRET: commercialisation of the 2RT® subthreshold nanosecond ophthalmic laser for retinal disease. It produced no material revenue in FY2025 or FY2026 (Appendix 4E, FY2025 and FY2026).

Independent characterisation

Nova Eye is economically a single-product, consumables-driven surgical device company. In FY2026, 100% of reported revenue (A$34.865 million) came from the Glaucoma Surgical Devices segment, and the large majority of that came from iTrack Advance in the USA (US$18.6 million of US$23.7 million group sales, about 78%).

Revenue model. Revenue is essentially all product revenue from single-use disposable devices sold per procedure to ambulatory surgery centres (ASCs), hospitals and ophthalmology practices. There is no material service, subscription or licensing revenue. The 2RT laser was historically sold as capital equipment with a planned per-use recurring fee, but it is currently dormant commercially pending a confirmatory US study. Management is exploring a licensing or partnership model for iTrack as a targeted ocular drug-delivery platform (Q1 FY2026 webinar, Nov 2025), but no revenue has been disclosed.

Value-chain position. Nova Eye is vertically integrated across R&D, regulatory, manufacturing and sales:

  • iTrack is manufactured in Fremont, California, and Molteno3 in Dunedin, New Zealand.

  • It sells directly in the USA and Germany. About 87% of last-twelve-month revenue at September 2025 came from its own sales teams in those two countries (Q1 FY2026 Appendix 4C).

  • It uses distributors in China and other markets.

Customer types. Glaucoma and cataract-glaucoma surgeons; ASCs and hospital outpatient departments; distributors (China and rest-of-world). In the USA, procedure economics are driven by Medicare facility and physician reimbursement.

End-markets served.

  1. Mild-to-moderate open-angle glaucoma: the MIGS or "interventional glaucoma" segment, standalone or combined with cataract surgery (iTrack/iTrack Advance).

  2. Severe or refractory glaucoma: tube shunts and glaucoma drainage devices (Molteno3).

  3. Intermediate age-related macular degeneration (iAMD) and potentially diabetic retinopathy (2RT, pre-commercial in the USA; CE-marked in Europe).

  4. Prospectively, ocular drug delivery (iTrack microcatheter, exploratory).

The business case rests on an under-penetrated procedure pool. Management cites roughly 30,000–35,000 US glaucoma surgeries per month for mild-to-moderate disease, of which iTrack holds about 3–5% (FY2026 results, 29 Jul and 26 Aug 2026). About 6 million US cataract patients a year have concurrent glaucoma (Sept 2024 quarterly).

Strategy

Stated strategy (themes from FY2025–FY2026 reporting)

  1. "Grow iTrack Advance in the USA." The USA accounts for most global interventional glaucoma revenue. Management frames the opportunity as penetrating the 30,000–35,000 monthly US mild-to-moderate glaucoma surgeries from a 3–5% share.

  2. Market activation and surgeon education. Investment in training, KOL podium presence (ASCRS, AAO, ISGS Masterclass Geneva, MIGS Symposium Montabaur, Canadian Glaucoma Society) and clinical data generation (CATALYST study, 24-month German data).

  3. Direct-market leverage. Direct markets (USA, Germany) earn superior margins versus distributor markets, and 87% of LTM revenue already came through direct channels (Q1 FY26).

  4. Operating leverage to profitability. Glaucoma-segment breakeven was reached in H2 FY25, group breakeven in H2 FY26, and positive EBITDA is targeted for FY27.

  5. Expansion via approvals. China iTrack Advance (NMPA, Sept 2025) through the established distributor.

  6. Platform optionality. iTrack for targeted ocular drug delivery with pharma partners; 2RT via AlphaRET with a partner-funded confirmatory study.

Initiatives register (last 24 months)

DateInitiativeDetailStatus
H2 FY2024 to FY2025US and German sales-team expansionFunded by the Feb 2024 and Jan 2025 raisesExecuted
Q1–Q2 FY2025Supply-chain remediationProduction cost issues in Q1 FY25 resolved in Q2 FY25Completed
FY2025 to FY2026Gross-margin programProduction efficiency and pricing discipline lifted GM from 66% to 70%Ongoing
Jul 2025Adelaide University quantum detection grantA$488kResearch
Sep 2025China iTrack Advance registrationNMPA approval; commercial launch via distributorFirst sales Q3 FY26
Nov 2025Drug-delivery partneringEvaluating iTrack microcatheter with pharma partnersExploratory; no timeline
FY2026CATALYST US clinical studyProspective study in mild-to-moderate POAGOngoing
FY2026Working-capital fundingA$2.75 million River Street loan facility replacing receivables facilityExecuted
ESGNo formal emissions or ESG targets disclosed——

Guidance

PeriodGuidanceOutcome
FY2025H2 FY25 sales (ex-China) US$9–10 million; glaucoma breakeven H2Met (H2 sales about US$10.4 million incl. China; glaucoma EBITDA about +US$65k)
FY2026 (initial, Jul 2025)Sales ex-China US$21–24 million; breakeven EBITDA H1 FY26 (later shifted to H2)—
FY2026 (upgraded, 5 May 2026)Sales ex-China US$22–23 millionAchieved: group sales US$23.7 million; H2 EBITDA positive
FY2027 (29 Jul 2026, reaffirmed 26 Aug 2026)Sales ex-China US$26–31 million; positive EBITDAPending

Implied FY2027 growth is about 13–35% on FY26 ex-China sales (FY26 ex-China not separately disclosed; computed on group US$23.7 million as an approximation, about 10–31%).

Medium-term targets beyond FY2027 have not been disclosed.

Products & Services

Glaucoma Surgical Devices segment

iTrack™ (original canaloplasty microcatheter)

Description: A flexible, illuminated microcatheter (about 200 µm diameter, with a fibre-optic lighted tip so the surgeon can visualise its position) inserted into Schlemm's canal and advanced 360 degrees. On withdrawal it delivers ophthalmic viscoelastic to dilate the canal and collector channels and to break up herniated tissue. This "pressurised viscodilation" is what management calls "angioplasty of the eye." Nothing is left in the eye and no tissue is removed. The company describes it as "stent-free, tissue-preserving, repeatable glaucoma surgery" (November 2025 investor presentation).

Indication: Reduction of IOP in adult patients with open-angle glaucoma, standalone or combined with cataract surgery.

Launch: Commercialised in 2008.

Status: Being superseded by iTrack Advance in the USA and Europe. Remained the product sold in China until NMPA approval of Advance (Sep 2025), with first Advance sales in China in Q3 FY2026. China iTrack sales were US$1.2 million in FY2025.

Pricing: Not publicly disclosed; sold per unit and reimbursed in the USA under canaloplasty CPT codes.

iTrack™ Advance (flagship)

Description: Next-generation iTrack that houses the microcatheter in an ergonomic, single-handed handpiece or injector. The surgeon advances and retracts the catheter with a thumb or forefinger wheel, removing the forceps manipulation required with the original device. This shortens operating time and lowers the learning curve, especially in combined cataract-glaucoma cases (Biotech Daily, Jun 2023; IBISWorld).

Regulatory: CE-marked and European roll-out from June 2022; US FDA clearance 1 April 2023; China NMPA registration 30 September 2025.

Clinical evidence: More than 170,000 patients treated with iTrack technology (Q1 FY2026 webinar; earlier figure of 120,000 surgeries, Jun 2023). A 24-month study by German surgeons showed about a 20% IOP reduction and near-elimination of medication. A US prospective CATALYST study is underway in mild-to-moderate primary open-angle glaucoma (Jan 2026 quarterly).

Target customer: Comprehensive and glaucoma ophthalmologists performing cataract surgery on patients with concurrent mild-to-moderate glaucoma, and standalone MIGS.

Pricing model: Per-unit disposable; ASP not disclosed.

Molteno3® Glaucoma Drainage Device platform

Description: A tube-shunt or glaucoma drainage device (GDD), derived from Professor Anthony Molteno's pioneering 1960s–70s work, that is permanently implanted to divert aqueous humour to a subconjunctival bleb plate. The platform includes various plate sizes, such as the Molteno3 SL (single-plate large) and SS (single-plate small) variants (NZ Optics, Aug 2020).

Indication: Severe, refractory or complex glaucoma, typically after failed prior surgery.

Manufacturing: Dunedin, New Zealand.

Acquired: 31 July 2020 for about A$0.921 million.

Strategic role: Completes a "full disease-spectrum" glaucoma bag for the direct sales force (iTrack for mild-to-moderate disease, Molteno3 for severe). Revenue is not separately disclosed and is believed to be a small minority of segment revenue.

AlphaRET segment

2RT® (Retinal Rejuvenation Therapy) laser

Description: A subthreshold, nanosecond-pulse (about 3 ns) ophthalmic laser designed to stimulate a biological healing response in the retinal pigment epithelium and Bruch's membrane without thermal damage to photoreceptors. It was developed on research by Prof John Marshall and a team led by Victor Previn (InDaily, Nov 2020).

Indications targeted: Intermediate AMD (to slow progression to late AMD); diabetic retinopathy/macular oedema (exploratory).

Evidence: The 2012–2018 LEAD trial (Centre for Eye Research Australia) did not meet its primary endpoint overall. It showed a signal of slowed progression in the subgroup of patients without reticular pseudodrusen. A confirmatory US study under an FDA IDE is required before US clearance.

Regulatory: CE Mark (Europe); about 40 trial units sold historically.

Commercial status: No material revenue in FY2025 or FY2026. AlphaRET is seeking a funding partner and management has not committed group capital to a pivotal trial.

Pricing: Historically capital sale plus planned per-use recurring fee; not currently active.

Pipeline and platform initiatives

InitiativeDescriptionStageSource
iTrack for targeted drug deliveryUsing the 360-degree microcatheter to deliver therapeutics to Schlemm's canal and suprachoroidal tissuesFeasibility with potential pharma partners; no definitive timingQ1 FY2026 4C and webinar
Next-generation iTrackFurther procedure-time reductions (announced in the FY2020 era; Advance was the first output)Commercialised as Advance; further iterations not disclosedInsight News 2020
Quantum-sensing early disease detectionA$488k grant with Adelaide UniversityResearchroic.ai summary, Jul 2025

Financial Narrative

All statutory figures in A$, continuing operations. Primary sources: Appendix 4E/Annual Reports FY2022–FY2026, FY results releases. Secondary: InvestSMART/Morningstar, Barchart (data from filings), Stoxray.

Income statement

Notes: - FY2022 revenue A$13.378 million (Stoxray; "just under A$13.4 million" per Biotech Daily); FY2021 revenue A$12.769 million, used for FY2022 growth.

  • FY2023 revenue A$17.025 million (Stoxray); InvestSMART shows A$17.5 million, which likely includes other income.

  • FY2023 EBITDA is derived from the FY24 release (FY24 loss of A$5.7 million was an A$2.9 million improvement); InvestSMART shows –A$8.71 million.

  • Net profit: FY2022 –A$7.496 million, FY2023 –A$15.293 million, FY2024 –A$8.790 million, FY2025 –A$9.059 million (Barchart, from filings); FY2026 –A$4.333 million (Appendix 4E FY2026). FY2023 includes about A$6.1 million of items below "net profit before abnormals" (InvestSMART: –A$9.2 million before, –A$15.3 million after), consistent with impairment.

  • EPS from InvestSMART. FY2026 implied basic EPS is about –1.5 A cents (computed: –A$4.333 million ÷ about 285 million shares) pending confirmation from the Annual Report.

  • Gross profit in A$ was not captured. Company-reported gross margin was about 83% in FY2022 (Kalkine), 66% in H1 FY2025, 70% in H2 FY2025 and 70% in H1 FY2026.

Margin profile

Computed from 6.1: Sources: H1FY25 report (sales A$12.925 million; EBITDA –A$4.237 million); FY25 presentation (GM 66% to 70%; opex/sales 88% to 70%); H1FY26 report (sales A$16.712 million; EBITDA –A$2.204 million; GM 70%); FY26 Appendix 4E (H2 EBITDA +A$172k). H2 values are derived as full year minus H1.

Revenue CAGR FY2022–FY2026 (A$): about 27% a year (A$13.4 million to A$34.9 million, computed). Company-reported constant-currency growth was 35% (FY24), 23% (FY25) and 26% (FY26). Management describes FY2026 as the fourth consecutive year above 25% in US$ terms.

Trend commentary. The income statement shows a classic medtech operating-leverage inflection. Between FY2023 and FY2026, revenue roughly doubled (+105%) while EBITDA losses shrank from about A$8.6 million to A$2.0 million. Three drivers stand out:

  1. The iTrack Advance launch in the USA from April 2023. US sales rose from about US$6.7 million (FY23, derived) to US$18.6 million (FY26).

  2. Gross-margin recovery. Supply-chain-driven production cost increases depressed H1 FY2025 margin to 66%. Process improvements, yield gains and "pricing discipline" restored it to 70%.

  3. Opex discipline. Opex as a share of sales fell from 88% to 70% across FY2025.

FY2023 was the trough: heavy US launch investment, depressed post-COVID volumes and impairment-type charges drove a –A$15.3 million net loss. The FY2026 net loss of A$4.3 million still reflects depreciation and amortisation (about A$2 million a year historically), interest on the working-capital facility, and share-based payments. Reported A$ growth (19%) lagged constant-currency growth (26%) in FY2026 because the A$ strengthened against the US$.

Balance sheet

Sources: Total assets from Barchart and InvestSMART. FY2025 cash A$5.055 million (Biotech Daily; ASX FY25: A$5.1 million); FY2024 cash derived from "down 18%" (about A$6.2 million). Debt and equity FY2025 from InvestSMART (total debt A$3.017 million, long-term A$2.383 million, equity A$18.967 million). FY2026 net assets A$14.275 million (Appendix 4E FY2026).

Liquidity events in FY2026.

  • Cash fell to A$1.2 million at 31 March 2026, with A$2.14 million of unused debt facilities (Q3 FY26 4C).

  • Liquidity at 30 June 2026 was about A$3.7–3.75 million of cash plus undrawn facilities (Q4 FY26 4C; FY26 results).

  • The company entered an A$2.75 million loan facility with River Street Nominees Pty Ltd, replacing the earlier receivables-backed working-capital facility. That facility had been secured by accounts receivable and tangible assets (Nov 2025 webinar; Appendix 4E FY2026).

  • Goodwill and intangibles: the balance-sheet split was not captured in reviewed sources. Intangibles relate to capitalised development and Molteno-related assets.

  • Working capital: not separately disclosed in reviewed sources. FY2022 current ratio was about 4.0x (Kalkine).

Commentary. The balance sheet has been eroding steadily since the post-divestiture peak: about A$26 million of cash at 30 June 2020, net of the A$0.29 per share distribution. Equity has been replenished three times with dilutive raises (2023, A$8 million in 2024, A$6.6 million in 2025). FY2026 net assets fell to A$14.3 million from A$19.0 million because no equity was raised and losses continued. The company now funds itself with a small secured loan. With EBITDA at breakeven, the balance sheet is adequate only if growth and margins continue as guided. Any setback would likely force another equity raise at a depressed price.

Cash flow

Sources: Operating cash flow FY2022–FY2024 from Stoxray (–A$4.683 million, –A$6.721 million, –A$7.857 million) and InvestSMART (FY2023 –A$6.82 million; FY2025 –A$6.15 million); ASX FY25 release (A$6.2 million outflow vs A$7.9 million). Financing values are rounded aggregator figures. FY2026 full-year operating cash flow was not captured; quarterly outflows were A$0.798 million (Q1) and A$1.2 million (Q3, affected by advance payments and FX).

Capex and free cash flow. Capex is not separately disclosed in reviewed sources and is small (investing outflow about A$1 million in FY2025). FY2025 free cash flow was about –A$7.2 million (operating –A$6.2 million plus investing –A$1.0 million, derived).

Commentary. Operating cash burn peaked in FY2024 (A$7.9 million) and has fallen every year since. Quarterly burn reached about A$0.8 million by Q4 FY2025 and Q1 FY2026, and Q3 FY2026 was temporarily worse because of supplier prepayments and currency. Management has warned that cash flow lags EBITDA because of working capital, including inventory build for China and receivables growth as US sales scale.

Key ratios

Computed from tables above except current ratio (Kalkine, FY2022). ROIC: Halo Technologies reported –36.4% (FY2024/25 basis). Interest coverage: negative (EBIT negative). Net debt/EBITDA and debt/equity: not meaningful (EBITDA negative through FY2025; net cash position through FY2025, with InvestSMART net gearing of –10.7%). Cash conversion cycle: not publicly disclosed.

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Financial Detail

Segment Overview

SegmentWhat it containsProductsStatus

Glaucoma Surgical Devices

Design, manufacture, marketing and sale of single-use glaucoma surgical devices; direct sales in USA and Germany; distributors elsewhere

iTrack™, iTrack™ Advance, Molteno3®

100% of FY2026 revenue

AlphaRET

Commercialisation of the 2RT® subthreshold nanosecond laser for retinal disease (iAMD, diabetic retinopathy)

2RT® laser system

No material revenue FY2025–FY2026

Revenue by Segment

Segment (AUD K)FY2024FY2025FY2026

Glaucoma Surgical Devices revenue

23,15729,07734,865

AlphaRET revenue

1681900

Group revenue (continuing)

23,32529,26734,865

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Segment Margins & Growth (%) and Revenue by Segment (%)

MetricFY2024FY2025FY2026

Glaucoma segment revenue growth YoY A$ (%)

362620

Glaucoma share of group revenue (%)

99.399.4100

Group sales growth constant currency (%)

352326

Segment EBITDA (AUD K)

Segment EBITDA (AUD K)FY2024FY2025FY2026

Glaucoma Surgical Devices EBITDA

-2,959—-709

Group EBITDA

-5,700-5,462-2,012

Income Statement and Margin Analysis (%)

MetricFY2022FY2023FY2024FY2025FY2026

Revenue (AUD Mn)

13.417.023.329.334.9

Revenue growth reported A$ (%)

4.927.337.025.519.1

Revenue (USD Mn, company-reported)

——15.318.823.7

EBITDA (AUD Mn)

—-8.6-5.7-5.5-2.0

Operating margin (%)

—-49.9-25.1-23.0—

Net profit after tax (AUD Mn)

-7.5-15.3-8.8-9.1-4.3

Basic EPS (A cents)

—-5.8-4.3-3.7—

Dividends per share (A cents)

00000

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Margin Analysis (%)

MetricFY2022FY2023FY2024FY2025FY2026

EBITDA margin (%)

—-50.6-24.5-18.7-5.8

Net margin (%)

-56.0-90.0-37.7-31.0-12.4

Income Statement and Margin Analysis (%) (H1FY2025–H2FY2026)

Half-year metricH1FY2025H2FY2025H1FY2026H2FY2026

Sales (AUD Mn)

12.916.216.718.2

Gross margin (%)

667070—

Group EBITDA (AUD Mn)

-4.2-1.3-2.20.2

Opex as % of sales

8870——

Balance Sheet and Per-Share Data

MetricFY2022FY2023FY2024FY2025FY2026

Total assets (AUD Mn)

36.630.429.926.5—

Cash and equivalents (AUD Mn)

——6.25.1—

Total debt incl. leases (AUD Mn)

———3.0—

Long-term debt incl. leases (AUD Mn)

———2.4—

Total equity / net assets (AUD Mn)

———19.014.3

Book value per share (AUD)

—0.120.090.07—

Retained earnings (AUD Mn)

—-21.9-30.7-39.7—

Cash Flow

MetricFY2022FY2023FY2024FY2025FY2026

Operating cash flow (AUD Mn)

-4.7-6.8-7.9-6.2—

Net investing cash flow (AUD Mn)

———-1.0—

Net financing cash flow (AUD Mn)

—6.06.06.0—

Dividends paid (AUD Mn)

00000

Share buybacks (AUD Mn)

00000

Returns & Leverage Ratios (%) and Financial Ratios (x)

RatioFY2022FY2023FY2024FY2025FY2026

ROA net loss / year-end total assets (%)

-20.5-50.3-29.4-34.2—

ROE net loss / year-end equity (%)

———-47.8-30.3

Asset turnover revenue / total assets (x)

0.370.560.781.11—

Current ratio (x)

4.04————

Revenue by Region

Region (USD Mn)FY2023FY2024FY2025FY2026

USA

6.711.414.218.6

China

——1.2—

Group total

—15.318.823.7

Revenue by Region (H1FY2025–Q2FY2026)

Region (USD K)Q2FY2025Q2FY2026H1FY2025H1FY2026

USA

3,3334,4986,4768,559

Germany

512503870877

Sales excluding China

4,0555,4707,67510,252

China

350603710603

Revenue by Region (LTM Dec2024–LTM Dec2025)

LTM to December (USD K)LTM Dec2024LTM Dec2025

USA

12,77716,272

Germany

1,7201,835

Sales excluding China

15,51619,895

China

1,3851,053

Revenue by Region (Quarterly)

Q1 comparison (USD K)Q1FY2024Q1FY2025

USA

2,4263,140

Germany

370367

China

0360

Margin Analysis (%) (FY2023–FY2025)

MetricFY2023FY2024FY2025

Total shareholder return fiscal year (%)

43.2-14.7-50.0

Share Price & Returns

Reference pointShare price (AUD)Source

Nov 2021 (AGM)

0.37

InvestSMART announcement history

Feb 2022

0.27

InvestSMART

Aug 2022 (FY22 results)

0.25

InvestSMART

May 2023 (placement)

0.18

Market Index

Mar 2024 (rights issue)

0.21

Market Index

Sep 2024

0.18

EODHD

Jan 2025 (placement)

0.12

ASX cleansing notice

Oct 2025

0.135

Biotech Daily

26 Feb 2026

0.16 before results, then 0.11–0.14

InvestSMART

29 Jul 2026

0.14 (+16.7% on day)

InvestSMART

26 Aug 2026

0.143 at release; 0.130 close

InvestSMART

Valuation Multiples

MultipleNova EyeBasis

Market capitalisation

About A$37 million (about US$24 million)

A$0.13 × about 285 million shares

EV / Sales (FY26)

About 1.0–1.1x

Market cap plus small net debt, divided by A$34.9 million revenue

P/E

n/m (loss-making)

—

EV / EBITDA

n/m (FY26 EBITDA negative)

—

P / B

About 2.6x

A$37 million ÷ A$14.3 million net assets

Stoxray P/S (May 2026)

1.40x

Stoxray

Capital Markets

ItemDetail

Analyst consensus

Limited coverage. Bell Potter hosted a company presentation (Nov 2025). Consensus estimates not publicly disclosed in reviewed sources. Simply Wall St reports analysts trimming revenue forecasts.

Dividend policy

No dividends; none expected while loss-making. Last distribution: A$0.29 special (Jul 2020).

Buybacks

None authorised

Credit ratings

Not rated by Moody's, S&P or Fitch

Debt maturity profile

A$2.75 million River Street Nominees facility (terms and maturity not captured); lease liabilities (FY25 total debt incl. leases A$3.0 million)

Index membership

Not in S&P/ASX 300 (historically included in ASX index rebalances as Ellex)

Liquidity

Average daily volume about 0.47–0.50 million shares (TipRanks, 2025)

Analyst Conclusions

Management guidance

FY2027 sales excluding China are guided at US$26–31 million, with positive full-year EBITDA. Management states it has sufficient liquidity (about A$3.75 million of cash and debt facilities at 30 June 2026) to support these targets (FY26 results, 26 Aug 2026). China upside from iTrack Advance sits on top of guidance.

Consensus

Formal consensus is not publicly disclosed. Guidance implies about 10–31% growth on FY26 group sales of US$23.7 million. The low end of guidance would represent the slowest growth in four years.

Bull case

  1. Operating leverage is now visible. EBITDA swung from –A$8.6 million (FY23) to +A$0.17 million (H2 FY26) while revenue doubled. At a 70% gross margin and opex/sales trending toward 70% or below, each additional US$1 million of US sales should drop roughly US$0.5–0.7 million to EBITDA. The mid-point of FY27 guidance could therefore deliver meaningful positive EBITDA and self-funding.

  2. Long US runway in a growing category. At about 4% of 30,000–35,000 monthly US procedures, doubling share to 8% would roughly double US revenue. Sight Sciences' 2025 stagnation suggests Nova Eye is winning canal-based share.

  3. Cheap optionality. Trading near 1x EV/Sales, the market assigns little value to China Advance, drug delivery or 2RT, any of which could re-rate the stock or attract a strategic acquirer.

Bear case

  1. Funding fragility. Net assets of A$14.3 million and A$1.2 million cash at March 2026 leave little margin. A quarter of slower US growth, a reimbursement shock or a China stocking reversal could force another dilutive raise at or below A$0.12.

  2. Reimbursement and competitive risk. Medicare LCD and fee-schedule changes are binary for a single-procedure company, and rivals have far larger evidence and sales budgets.

  3. Structural margin and scale gap. At 70% gross margin versus 86% at Sight Sciences, and with Germany flat, the business may plateau at a sub-scale level. Guidance as low as US$26 million implies decelerating growth.

Catalysts and monitorables (next 12 months)

Expected timingCatalyst / monitorable
By 31 Oct 2026Q1 FY27 Appendix 4C: US growth rate, EBITDA, cash
29 Oct 2026AGM: director elections, remuneration vote, trading update
Nov 2026CY2027 Medicare final rules (OPPS/ASC and physician fee schedule) affecting canaloplasty payment
Nov 2026 – Jan 2027China iTrack Advance orders and launch progress
Jan–Feb 2027Q2 FY27 4C and H1 FY27 results: confirmation of positive EBITDA
FY2027CATALYST study data; additional peer-reviewed publications
FY2027Any drug-delivery partnership or AlphaRET 2RT partner announcement
OngoingUse of the River Street facility; any equity raise

Analyst verdict

Nova Eye Medical has completed the hardest part of its post-Ellex reinvention. Six years after selling its laser business for A$100 million, it has turned a pandemic-battered iTrack franchise of about A$13 million in revenue into a A$34.9 million (US$23.7 million) business. Growth has exceeded 25% for four straight years, gross margin has recovered to about 70%, and the company reached its first EBITDA-positive half in H2 FY2026. The engine is clear and credible: iTrack Advance in the US, sold directly into a large, under-penetrated pool of mild-to-moderate glaucoma surgeries where Nova Eye holds only 3–5% share. The evidence base is improving, and the company appears to be taking share from its closest canal-based competitor, Sight Sciences, whose interventional-glaucoma revenue was flat in 2025.

The equity story is nonetheless constrained by balance-sheet arithmetic. Net assets have shrunk to A$14.3 million, cash dipped to A$1.2 million in March 2026, and liquidity depends on a modest A$2.75 million secured loan plus continued breakeven trading. Shareholders have absorbed three raises since 2023, the latest at A$0.12, and the share price, at about A$0.13, sits roughly where that raise was priced despite a more than 50% increase in revenue since. The market is treating Nova Eye as a funding risk rather than a growth asset.

FY2027 is therefore a "prove-it" year. If the company delivers sales near the mid-point of its US$26–31 million guidance with positive EBITDA and stable US reimbursement, the funding overhang should lift. At about 1x EV/Sales the stock would then look mispriced against peers and potential strategic acquirers. Failure on any of those three fronts would likely mean further dilution. On balance, the risk/reward is asymmetric but highly execution-dependent.


Source index (primary unless noted)

  • ASX releases (announcements.asx.com.au): FY24 results (26 Aug 2024); Sept 2024 quarterly (31 Oct 2024); H1 FY25 (26 Feb 2025); FY25 results (27 Aug 2025); Record December quarter (12 Jan 2026); Q2 FY26 4C (29 Jan 2026); H1 FY26 (26 Feb 2026); Guidance upgrade (5 May 2026); FY20 results (28 Aug 2020); March 2023 investor presentation

  • ASX releases via InvestorPA, InvestSMART and Webull: NMPA approval (30 Sep 2025); Q1 FY26 4C (31 Oct 2025); Q3 FY26 4C (29 Apr 2026); Q4 FY26 4C (29 Jul 2026); FY26 Appendix 4E and results (26 Aug 2026); AGM notice (3 Sep 2026); Q4 FY25 4C (29 Jul 2025); FY25 Appendix 4E (27 Aug 2025); cleansing notice (7 Feb 2025)

  • Q1 FY26 investor webinar transcript (roic.ai, Nov 2025); November 2025 investor presentation (Bell Potter-hosted)

  • Sight Sciences Q4/FY2025 results (SEC Form 8-K exhibit 99.1, 2026)

  • Secondary: Market Index; InvestSMART financials; Morningstar via Motley Fool; Barchart; Stoxray; EODHD; Halo Technologies; Kalkine (Dec 2022; Jul 2026); Biotech Daily (Jun 2023; Oct 2025); InDaily (May and Nov 2020); Insight News (2020); mivision (2020); NZ Optics (Aug 2020); CRSToday (2020); TipRanks; Moomoo/MT Newswires; IBISWorld; Plunkett Research

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Executive Leadership

Board of Directors

NameRoleTenureBackgroundSource

Victor Previn

Executive Chairman

Director since 16 Jul 2001; Chair since Jul 2005; MD 2003–2005

Professional engineer and co-founder of Ellex (1985); more than 35 years in ophthalmic lasers and devices; led the 2RT research program; also director of Havilah Resources (ASX: HAV)

Morningstar/Motley Fool; InvestSMART; TipRanks

Tom Spurling

Managing Director (CEO)

Ellex CEO 2011–2019; Nova Eye director from 2020; MD

Former Ellex CEO; led the Lumibird sale and the pivot to glaucoma consumables

InDaily, Nov 2020; ASX releases

Daniel Webb

Non-executive Director

Not confirmed

Not confirmed in reviewed sources

Biotech Daily, Oct 2025

Rahmon Coupe

Non-executive Director

Not confirmed

Not confirmed in reviewed sources

Biotech Daily, Oct 2025

Mike Southard

Non-executive Director

Not confirmed

Not confirmed in reviewed sources

Biotech Daily, Oct 2025

Executive Leadership Team

NameRoleNotes

Tom Spurling

Managing Director

Primary company spokesperson

Mark Flynn

Investor Relations

Hosts quarterly webinars

Joe Bankovich

President, Nova Eye Medical, Inc. (US) (as of 2020)

—

CFO / Company Secretary

Not confirmed in reviewed sources (Simon Gray was Company Secretary in Aug 2020)

ASX FY20 release

Prof John Marshall

Board member, AlphaRET Pty Ltd

CRSToday, 2020

Major Shareholders

HolderShares% of issued capitalAs atSource

Victor Previn (total relevant interest)

11,822,201

about 4.2

30 Jun 2025

Market Index

of which Sedico Pty Ltd (Previn Family A/C)

7,945,3552.792,025

Market Index / Morningstar

of which Sedico Pty Ltd (Previn Superfund A/C)

2,258,3730.792,025

Market Index / Morningstar

Australian Ethical Investment (via National Nominees)

40,113,310

17.53 (then)

15 Mar 2024

Market Index substantial holder notice

National Nominees Ltd (custodian)

35,438,32518.62

30 Jun 2023

Market Index Top 20

J P Morgan Nominees Australia (custodian)

15,386,7788.08

30 Jun 2023

Market Index Top 20

Competitive Landscape

Key Competitors

CompetitorSegment overlapKey productsLatest revenuePositioning vs Nova Eye

Glaukos Corp (NYSE: GKOS)

MIGS (trabecular bypass); sustained drug delivery

iStent inject W, iStent infinite, iDose TR

—

Category leader; scale, reimbursement and pharma adjacency far exceed Nova Eye

Sight Sciences (NASDAQ: SGHT)

Canaloplasty and trabeculotomy (closest direct competitor)

OMNI Surgical System, SION

FY2025 revenue US$77.4 million (–3%); Interventional Glaucoma US$75.7 million; GM 86%; net loss US$38.4 million

Head-to-head in canaloplasty; about 3x Nova Eye's revenue; facing growth stall that Nova Eye has exploited

Alcon (NYSE/SIX: ALC)

MIGS (Schlemm's canal scaffold); SLT lasers; cataract channel

Hydrus Microstent (from Ivantis acquisition)

Group revenue about US$10 billion (FY2024); Hydrus not separately disclosed

Bundles MIGS with cataract equipment and IOLs; enormous channel

AbbVie (Allergan) (NYSE: ABBV)

Subconjunctival MIGS / bleb surgery

XEN Gel Stent

—

More advanced disease; overlaps with Molteno3 indications

Santen Pharmaceutical (TSE: 4536)

Bleb-forming MIGS

PreserFlo MicroShunt

—

Europe/Japan strength

New World Medical (private)

Goniotomy and GDDs

Kahook Dual Blade, Ahmed Glaucoma Valve

—

Direct competitor to Molteno3 (Ahmed) and to iTrack (KDB goniotomy)

Johnson & Johnson Vision (NYSE: JNJ)

GDDs

Baerveldt glaucoma implant

—

Competes with Molteno3

iSTAR Medical (private, Belgium)

Supraciliary MIGS

MINIject

—

Emerging, mainly EU

Elios Vision (private)

Excimer laser trabeculostomy

ELIOS

—

New US entrant (FDA cleared) in combined-cataract MIGS

MicroSurgical Technology (private)

Ab-interno trabeculotomy

Trabectome

—

Legacy competitor

Lumibird / Ellex and other SLT vendors

First-line laser therapy (SLT)

Tango SLT lasers

Lumibird group revenue not separately allocated

Substitute: earlier-line laser therapy delays surgery

Pharma (topical drops; sustained release)

Medication alternative

Prostaglandin analogues; Durysta (AbbVie); iDose TR (Glaukos)

—

Substitutes; iTrack positions on medication elimination

“—” = not publicly disclosed.

Peer Comparison FY2026

MetricNova Eye (FY2026, Jun YE)Sight Sciences (FY2025, Dec YE)Glaukos (FY2024, Dec YE)

Revenue (USD Mn)

23.777.4383.5

Revenue growth (%)

26-3—

Gross margin (%)

about 70

86—

EBITDA / profitability

Group EBITDA –A$2.0 million FY; H2 positive

Net loss US$38.4 million

Not captured

R&D (USD Mn)

—14.6

Not captured

R&D % of revenue

—18.9

Not captured

“—” = not publicly disclosed.

Recent Developments

Leadership changes, litigation, layoffs and regulatory actions: none disclosed in the period.*

Company Snapshot

$23.7M

Revenue

50

Employees

1985

Founded

South Australia, Australia

Headquarters

SWOT Analysis

Strengths

  • Sustained high growth: Four consecutive years of sales growth above 25%; FY2026 sales US$23.7 million (+26%) (Q4 FY26 4C, 29 Jul 2026).
  • US traction: US sales of US$18.6 million in FY2026 (+30%), up from about US$6.7 million in FY2023, with six or more consecutive half-years of growth at about 40% CAGR (Jan 2026 release).
  • Profitability inflection: First EBITDA-positive half (H2 FY2026, +A$172k); full-year EBITDA loss improved by A$3.5 million to A$2.0 million (Appendix 4E FY26).
  • Gross-margin recovery: 66% (H1 FY25) to 70% (H2 FY25 and H1 FY26) through production efficiency and pricing discipline (H1 FY26 report).
  • Direct-channel economics: 87% of LTM revenue at Sept 2025 came through own sales teams in the USA and Germany (Q1 FY26 4C).
  • Differentiated, evidence-backed procedure: More than 170,000 patients treated; 24-month data showing about 20% IOP reduction with near-elimination of medications (Q1 FY26 webinar).
  • Regulatory breadth: iTrack Advance approved in the EU (2022), US (FDA, Apr 2023) and China (NMPA, Sep 2025).

Weaknesses

  • Sub-scale revenue: US$23.7 million versus Sight Sciences' US$77.4 million (FY2025) and Glaukos' about US$383.5 million (FY2024).
  • Weak balance sheet: Net assets fell to A$14.275 million (FY26); cash was A$1.2 million at 31 Mar 2026 (Q3 FY26 4C).
  • Persistent statutory losses: Net loss A$4.3 million in FY2026 after A$9.1 million (FY25) and A$15.3 million (FY23); retained losses about –A$39.7 million at FY25 (InvestSMART).
  • Gross margin below peers: 70% versus 86% at Sight Sciences (FY2025).
  • Product concentration: 100% of FY2026 revenue from one segment, overwhelmingly iTrack (Appendix 4E FY26).
  • Germany stagnation: Q2 FY26 sales of US$503k (–2%) despite investment in the local team (Jan 2026 release).
  • Governance: Executive Chairman with 25-year tenure; no independent chair (ASX Recommendation 2.5).

Opportunities

  • US penetration runway: Only about 3–5% of 30,000–35,000 monthly US procedures (FY26 presentation).
  • China upgrade cycle: Advance approved Sep 2025, first sales Q3 FY26; China original-iTrack revenue was US$1.2 million in FY25 (NMPA release).
  • FY2027 guidance: US$26–31 million ex-China with positive EBITDA; delivery would remove funding overhang (FY26 results).
  • Drug-delivery platform licensing with pharma partners (Q1 FY26 4C).
  • 2RT partnering via AlphaRET for a US pivotal study in iAMD, a large unmet need (AlphaRET 2020 materials).
  • Strategic M&A interest: Sight Sciences' 2025 revenue decline and incumbent interest in canal-based procedures could make Nova Eye a bolt-on target (speculative).
  • Clinical data catalysts: CATALYST US study results could support adoption and reimbursement (Jan 2026 quarterly).

Threats

  • Reimbursement changes: Proposed MAC MIGS LCD changes caused "temporary market confusion" in early 2025 (H1 FY25 report).
  • Competitive bundling by Alcon (Hydrus with cataract portfolio) and pharma alternatives (iDose TR, Durysta).
  • Dilution risk: Three equity raises from 2023 to 2025, including A$0.12 in Jan 2025 (ASX cleansing notice).
  • China channel risk: LTM China sales –24% to US$1.05 million (Dec 2025) with lumpy shipments.
  • FX headwinds: FY26 reported growth was 19% in A$ versus 26% in constant currency (Appendix 4E FY26).
  • Supply-chain fragility: Q1 FY25 production cost issues depressed gross margin (H1 FY25 report).

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Key Developments

DateEventSignificance
Mar 2025Tranche 2 of A$6.6 million placement issued after shareholder approval, including A$49,999 subscribed by the Chairman Market Index director tradesCompleted recapitalisation for FY2026
29 Jul 2025Q4 FY25 4C: record FY25 revenue A$29.2 million (US$18.8 million); Q4 sales A$8.8 million (record); glaucoma EBITDA +US$65k in H2 FY25 ASX Q4 FY25 4CFirst segment-level breakeven
29 Jul 2025Amended 4C lodged same day InvestorPAAdministrative correction
Jul 2025Adelaide University quantum grant (A$488k) roic.aiNon-dilutive R&D
27 Aug 2025Audited FY25 results: revenue A$29.3 million (+23%); US sales US$14.2 million (+26%); cash A$5.1 million; FY26 guidance US$21–24 million ex-China ASX FY25 resultsConfirms trajectory
27 Aug 2025FY25 investor presentation: GM 66% to 70%; opex/sales 88% to 70% InvestorPAOperating leverage evidence
30 Sep 2025NMPA approves iTrack Advance in China ASX releaseUnlocks next-generation product in largest distributor market
31 Oct 2025Q1 FY26 4C: sales ex-China +32% to US$4.9 million; LTM revenue more than A$30 million; operating outflow A$0.798 million ASX Q1 FY26 4CMomentum and burn reduction
Oct 2025China shipment slips from September into October Q1 FY26 webinarIllustrates China lumpiness
4–5 Nov 2025Investor webinar: reimbursement update, 24-month iTrack Advance paper, drug-delivery update Webinar transcriptClinical credibility; platform optionality
Nov 2025Investor presentation "Stent-Free, Tissue-Preserving, Repeatable Glaucoma Surgery" Bell Potter-hosted deckRepositions brand within interventional glaucoma
12 Jan 2026Record December quarter: H1 FY26 sales US$10.9 million (+29%); six consecutive halves of US growth (about 40% CAGR) ASX releaseGrowth confirmation
29 Jan 2026Q2 FY26 4C with regional table; clinical and conference activity (ISGS Geneva, MIGS Symposium Montabaur, CGS Canada) ASX Q2 FY26 4CTransparency on regions
26 Feb 2026H1 FY26 results: revenue A$16.7 million (+29%; +31% cc); EBITDA loss A$2.2 million (improved A$2.0 million); GM 70%; loss after tax A$3.365 million ASX H1 FY26Margin recovery
26 Feb 2026Share price falls from A$0.16 to the A$0.11–0.14 range after results InvestSMARTMarket sceptical despite progress
Mar 2026Record US monthly sales; first iTrack Advance sales in China Q3 FY26 4CInflection in both key markets
29 Apr 2026Q3 FY26 4C: sales US$5.8 million (+23%); EBITDA loss US$75k; cash A$1.2 million plus A$2.14 million unused facilities; weather headwinds early in quarter ASX Q3 FY26 4CLiquidity tight, but near breakeven
30 Apr 2026Investor webinar announced for 5 May 2026 ASX releaseIR cadence
5 May 2026Record April US sales; FY26 guidance upgraded to US$22–23 million ex-China; LTM US$22.8 million (+26%); first positive "EBITDA from operations" US$138k (Q3) ASX releaseGuidance upgrade
29 Jul 2026Q4 FY26 4C: FY26 sales US$23.7 million (+26%); USA US$18.6 million (+30%); H2 EBITDA +US$0.14 million; FY27 guidance US$26–31 million ex-China; liquidity A$3.7 million ASX Q4 FY26 4C; KalkineFour straight years of growth above 25%; first EBITDA-positive half
29 Jul 2026Share price +16.7% to A$0.14 InvestSMARTPositive reaction
26 Aug 2026Appendix 4E and Annual Report FY26: revenue A$34.865 million (+19% reported); EBITDA loss A$2.012 million; H2 EBITDA +A$172k; net loss A$4.333 million; net assets A$14.275 million ASX/InvestorPAAudited confirmation
26 Aug 2026River Street Nominees A$2.75 million loan facility disclosed (replaces receivables facility) Appendix 4E FY26Non-dilutive liquidity
26 Aug 2026FY26 investor presentation: iTrack used in about 3–5% of US mild-to-moderate glaucoma surgeries; FY27 positive EBITDA targeted InvestSMARTScale of runway
3 Sep 2026AGM date set for 29 Oct 2026; director nominations closed 10 Sep 2026 ASX releaseGovernance event
Sep 2026Notice of AGM scheduled for dispatch ASX releaseRemuneration and director resolutions

Financial Performance

Explore key financial metrics, segmented revenue, balance sheet health, and performance trends.

Revenue

6 charts
Revenue by Segment: Glaucoma Surgical Devices revenue rose from AUD 23.2 Mn in FY2024 to AUD 34.9 Mn in FY2026.
Nova Eye Medical Limited — Revenue by Segment
Series (AUD Mn)FY2024FY2025FY2026
Glaucoma Surgical Devices revenue23.229.134.9
AlphaRET revenue0.20.20
Group revenue (continuing)23.329.334.9

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