Retinal Prosthesis Companies (Schema, Aug 2026)

What: Current major companies in retinal/visual prostheses — device type, channels, status, regulatory. Companion to retinal-prosthesis and brain-computer-interface.

Company schema

Subretinal

CompanyHQDevice (type · channels)Status (2026-08)Key facts
Science Corporation (ex-Pixium Vision)Alameda, CA, USPRIMA — subretinal photovoltaic · 378 pixels (2×2 mm)Commercial (EU)Founded 2021 by max-hodak; acquired Pixium PRIMA IP Apr 2024; CE mark (MDR/DEKRA) + EU launch Jul 22 2026; FDA Breakthrough (2023) + 2× HUD (Jul 2026); 1.5B valuation (Mar 2026); NEJM 2026 trial: 81% improved ≥0.2 logMAR, 84% read letters; see science-corp
Pixium Vision (PRIMA origin)Paris, FR (EU)PRIMA — subretinal photovoltaic · 378 pixels; IRIS I (epiretinal)Acquired (liquidated)Founded 2011 (Institut de la Vision/UPMC spin-out); first-in-human 2017; FDA IDE 2018; first US implant UPMC 2020; closed Jan 2024 → Science Corp.; see pixium-vision
Retina Implant AGReutlingen, DEAlpha IMS / Alpha AMS — subretinal · 1,500 electrodes (3×3 mm)DefunctCE mark 2013; largest electrode count of its era; shareholders dissolved company 19 Mar 2019 — implanted patients left abandoned
Nano RetinaHerzliya, ILNR600 — subretinal (penetrating epiretinal, NIR-powered)Inactive9 patients; trial NCT04295304 terminated end-2023 (lack of funding); Yanovitch et al. bioRxiv 2022
Iridium Medical Technology (晶祈生技)Hsinchu, TWHARP4k — subretinal · ~4,000 pixels (30 µm, flexible contact-lens shape)PreclinicalFounded 2012 by Long-Sheng Fan; US9114004B2 (flexible artificial retina, 2015); Diamond Biofund; ~$5.68M raised; highest pixel count of any design worldwide; VP: Feng-Hsiung Hsu (IBM Deep Blue); see iridium-medical
Boston Retinal Implant ProjectBoston, MA, US (commercial partners: Bionic Eye Technologies + Visus Technology)Subretinal — 256+ ch, wirelessPreclinicalTitanium case on sclera; thin flexible electrode array only enters eye; 256+ independently configurable stimulation channels; bostonretinalimplant.org
AxorusParis, FRPhotoacoustic film (PDMS/CS/PDMS) — subretinal · 51-µm acoustic pixelsPre-clinicalBU/INSERM spin-out; patents licensed from BU; developing contact-lens form factor; COI (Moulet/Losasco = major stakeholders); first-in-human safety study planned; see axorus

Epiretinal

CompanyHQDevice · channelsStatus (2026-08)Key facts
Cortigent (ex-Second Sight)Valencia, CA, USArgus II — epiretinal · 60 ch (discontinued); Orion — cortical · 60 chActive (pivot to cortical)Argus II: CE 2011, FDA 2013 (first FDA-approved); production halted 2019, patients unsupported; Cortigent = Vivani Medical subsidiary (2023); S-1 filed (Nasdaq: CRGT). IEEE Spectrum (Feb 2022) documented >350 abandoned implantees — patients couldn’t get MRIs, crowd-sourced spare parts; FDA postapproval study recorded 36 serious adverse events in 30 patients (2007–2019); Second Sight merged with Nano Precision Medical in 2022. 1
IntelliMicro Medical (微智医疗)Changsha, CN / Pasadena, CA, USIMIE 256 — epiretinal · 256 ch (248+8 electrodes, Parylene-C)ClinicalFounded Mar 2018 by Caltech/Golden Eye Bionics (Humayun, Tai, Grubbs); first-in-human 5 RP patients 2021 (99.9% electrode survival); Jun 2026 Xiangya Hospital: first totally blind Chinese subject → character recognition + independent walking (Prof. Xu Huizhuo, Humayun guidance); fully domestic IP; Hunan provincial funding; see intellimicro-medical
Nanochap (暖芯迦)Hangzhou, CNRetinal visual BCI — epiretinal · 320 ch (3D pillar electrodes, 50 µm)Clinical (GCP trial)Founded 2014 (Univ. Melbourne spinout); CEO Yang Jiawei; ¥300M (~$41M) raised May 2026 (Legend Capital, Tencent); China first high-res retinal BCI: patient “Lingling” saw on day 2 post-op; 256-level grayscale; >10 yr hermetic lifespan; magnetic fixation; see nanochap
RWTH Aachen UniversityAachen, DEEPI-RET 3 — epiretinal · 25 ch (fully intraocular)Historical (clinical, completed)6 patients; removed at 1 month per ethics guidelines; no AEs; VA light perception to hand motion; IOP coil embedded in IOL — no transscleral wire; Menzel-Severing et al. Eye 2012;26(4):501-509
Polyretina (Ghezzi lab, EPFL/USI)Lugano, CHPolyretina — foldable photovoltaic epiretinal, wide-fieldPreclinicalActivates RGCs at safe irradiance; moldable for full retinal surface coverage; 2-yr in vitro lifetime; no cytotoxicity; Ferlauto et al. Nat Commun 2018;9:992. doi:10.1038/s41467-018-03386-7

Suprachoroidal

CompanyHQDevice · channelsStatus (2026-08)Key facts
Bionic Vision Technologies (BVT)Melbourne, AUSuprachoroidal — 44-ch gen 2 (44 Pt electrodes, postauricular headpiece)Active (clinical)World’s first suprachoroidal visual prosthesis; phase 2 (4 patients): safety confirmed, meaningful functional improvements; FDA Breakthrough Device designation; no commercial approval; Petoe et al. TVST 2021;10(10):12
Phoenix99 (Bionics Institute / U. Sydney)Melbourne/Sydney, AUPhoenix99 — suprachoroidal · 98 stimulation sites + 1 common electrodePreclinicalBovine in vivo model: safety confirmed; 98-channel prosthesis in scleral pocket; Eggenberger et al. Biomaterials 2021;279:121191
Osaka University (Fujikado group)Osaka, JPSuprachoroidal-transretinal stimulation — 49-microelectrode arrayResearch (in vivo studies)3 patients; favorable safety profile; variable functional results; scleral pocket placement; not commercialized; Fujikado et al. IOVS 2011;52(7):4726-4733. (Previously listed as “Nidek STS” — Nidek is a separate company; device is from Osaka University group)

Optic Disc

GroupHQDeviceStatusKey facts
Osaka University Medical School (Sakaguchi/Nishida group)Osaka, JPAV-DONE (Artificial Vision by Direct Optic Nerve Electrode)Clinical (2 patients total)Gen 1 (2009): 1 patient; phosphenes confirmed but device dislodged repeatedly. Gen 2: 7 stim + 1 ref electrodes; 1-step implantation; tested in rabbits + 1 human volunteer (6/7 electrodes evoked phosphenes, no complications). Unique placement: stimulates optic disc, bypasses entire retina. Sakaguchi et al. J Artif Organs 2009;12(3):206. Nishida et al. Brain Stimul 2015;8(3):678-681.

Transcorneal electrical stimulation (TES — therapy, not a prosthesis)

Adjacent to the implant companies: stimulation therapy aiming to slow degeneration / preserve remaining vision in RP — no phosphenes, no form vision, nothing implanted. Included here because it occupies the “electrical stimulation of the retina” niche left vacant by the defunct implant makers and shares the RP patient population.

CompanyHQDevice (type · channels)Status (2026-09)Key facts
Okuvision GmbH (ex-Retina Implant AG subsidiary)Kusterdingen, DEOkuStim® — transcorneal electrical stimulation (TES), non-invasive home therapy · no electrodes implantedCommercial (EU)Founded end-2007 as Retina Implant AG subsidiary (now independent); co-developed with Tübingen University Hospital ophthalmology; CE mark Class IIa 2014; OkuStim® 2 approved 2025; RP studies since 2011 (safety/efficacy, visual-field endpoints); glaucoma study protocol in BMJ Open (Mar 2026); CEO Dr. Alfred Stett; okuvision.de

Distinction: every row above delivers a visual percept via an implanted array; OkuStim delivers neuroprotective stimulation of surviving retina — the successor path of the same Tübingen ecosystem that produced the Alpha IMS/AMS implants (Retina Implant AG dissolved 2019).

Dimensions of comparison

  • Placement: subretinal (PRIMA, Alpha AMS, NR600, HARP4k, Boston Retinal Implant, Axorus) — stimulates bipolar cells, needs intact inner retina; epiretinal (Argus II, IMIE 256, EPI-RET 3, Polyretina) — stimulates RGCs, simpler surgery but axonal stimulation distorts mapping; suprachoroidal (BVT, Phoenix99, Osaka STS) — safest placement, more remote stimulation, lower resolution per channel; optic disc (AV-DONE) — bypasses entire retina, unique for RP; cortical (Orion, Gennaris, Blindsight, ICVP, Biomedical Technologies) — works even where optic nerve is damaged.
  • Regulatory/commercial reality: Only PRIMA has reached commercial availability as a visual prosthesis (EU, CE-marked, form vision). Every other implant product either died (Argus II, Alpha AMS, NR600) or remains clinical/preclinical. The one other CE-marked commercial product in this table is not a prosthesis at all: OkuStim® TES therapy (Class IIa, 2014; OkuStim 2 2025) sells neuroprotective stimulation, not vision.
  • Funding: Science Corp 650M+ Series E (2025); Nanochap ¥300M (~5.68M (Diamond Biofund); most others million-scale (BVT, Nano Retina) — consolidation is the norm (Pixium → Science; Second Sight → Cortigent/Vivani).
  • Channel count as a rough resolution proxy: 25 (EPI-RET 3) → 44–60 (BVT gen 2, Argus II, Orion) → 98 (Phoenix99) → 256 (IMIE 256, Boston RI) → 320 (Nanochap retinal BCI) → 378 pixels (PRIMA) → 1,500 electrodes (Alpha AMS) → ~4,000 pixels (HARP4k, preclinical) → ~51 µm acoustic pixels (Axorus/photoacoustic, no discrete channel count — spatially continuous).

Verdict

The field has consolidated to one commercial leader (Science Corp/PRIMA, EU CE-marked), with a wide tier of preclinical challengers (Axorus photoacoustic, IMIE 256, Boston Retinal Implant, Phoenix99) and a graveyard of technically-successful-but-commercially- failed devices (Argus II, Alpha AMS, NR600). Success requires not just approval but reimbursement — and, as Hodak argues, the disease-first (GA/AMD, >5M patients) strategy is the fastest path. The Optic Disc (AV-DONE) approach remains a niche curiosity with very limited patient numbers. Off-implant, the Tübingen ecosystem (Retina Implant AG’s successor Okuvision) pivoted to non-invasive OkuStim® TES therapy — the only other CE-marked commercial product in this schema, selling neuroprotection rather than vision. See max-hodak and science-corp.

Cortical alternative: for blindness caused by optic-nerve/inner-retina damage, cortex-interfacing devices are the universal option — see cortical-visual-prosthesis-companies.

References

Footnotes

  1. raw/articles/ieee-spectrum-argus-obsolete-2022.md