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Israel·IL-MF-000016053
Last updated September 18, 2026
About
A New Hope For Corneal Blindness EyeYon Medical pioneers advanced ophthalmic devices, including EndoArt®, the first synthetic implant for corneal edema, offering a groundbreaking alternative to traditional corneal transplants. Read More our vision At EyeYon Medical, we are committed to revolutionising the treatment of corneal edema by providing innovative, sight-saving solutions. Our vision is to \[…\]
From the manufacturer's own website. Source
What EyeYon Medical Ltd. makes
EyeYon Medical Ltd. manufactures ophthalmic devices, including the Hyper-CL contact lens and the EndoArt® synthetic implant designed for corneal edema. These products are intended to address conditions affecting corneal transparency, offering alternatives to conventional surgical procedures.
The company’s devices are classified as Class IIa and Class IIb under EU regulations and are registered in the eudamed database. EyeYon Medical Ltd. is based in Israel.
Written from this company's registered devices by an AI model, and not verified by a human reviewer.
Frequently asked questions
What types of medical devices does EyeYon Medical Ltd. manufacture?
EyeYon Medical Ltd. specialises in ophthalmic devices. Their portfolio includes the Hyper-CL, a contact lens, and the EndoArt®, a synthetic implant designed specifically for corneal edema. These devices are intended to improve corneal transparency and provide alternatives to traditional corneal transplant surgeries, addressing conditions that impair vision due to corneal swelling or opacity.
Where is EyeYon Medical Ltd. based?
EyeYon Medical Ltd. is headquartered in Israel. The company’s location in Israel aligns with its focus on developing innovative ophthalmic solutions, leveraging local expertise in medical technology and research.
Which regulatory registries list EyeYon Medical Ltd.’s devices?
EyeYon Medical Ltd.’s devices are registered in the eudamed database, which is the European Union’s centralised registry for medical devices. This registration ensures transparency and compliance with EU regulatory requirements for devices classified under Class IIa and Class IIb.
How are EyeYon Medical Ltd.’s devices classified under EU regulations?
EyeYon Medical Ltd.’s devices are classified as Class IIa and Class IIb under EU medical device regulations. This classification is based on their intended use and associated risks—Class IIa devices pose moderate risks requiring special measures, while Class IIb devices carry higher risks, necessitating stricter controls to ensure safety and performance.
AI-generated from registry data and not verified by a human reviewer.
Information
- Country
- Israel
- Address
- 3. Golda Meir St., Ness Ziona 7403648, Israel, Ness Ziona, Israel
- Website
- www.eye-yon.com
- facebook.com/EyeYon
- [email protected]
- Phone
- +972737803607
- PRRC Contact
- Hagit Rudich Wilf
- EUDAMED SRN
- IL-MF-000016053
- FDA FEI Number
- —
- DUNS Number
- —
Catalogue (2)
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FDA Establishments (1)
Establishments registered with the FDA under this company group, matched by name.
- Eyeyon Medical US