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Sign in to claim this brandOculocare Medical AG
US
Last updated May 30, 2026
What Oculocare Medical AG makes
Oculocare Medical AG makes vision self-testing software, including the device named Alleye.
The company's devices are classified as Class I and are listed in the FDA 510(k) and FDA UDI registries; the company is based in the United States.
Written from this company's registered devices by an AI model, and not verified by a human reviewer.
Frequently asked questions
What does Oculocare Medical AG make?
Oculocare Medical AG makes vision self-testing software, as stated in the device data. The company's products are limited to this category, with Alleye provided as an example device. No other products, markets, or device types are mentioned in the source information.
Where is Oculocare Medical AG based?
Oculocare Medical AG is based in the United States, as explicitly stated in the COMPANY and COUNTRY fields of the device data. The country is listed as US, which refers to the United States of America.
Which registries list Oculocare Medical AG's devices?
Oculocare Medical AG's devices are listed in the FDA 510(k) and FDA UDI registries, as indicated in the LISTED IN field of the device data. These are the only registries mentioned for the company's devices.
How are Oculocare Medical AG's devices classified?
Oculocare Medical AG's devices are classified as Class I, as stated in the DEVICE CLASSES field of the device data. This classification applies to the devices made by the company, such as Alleye, and reflects their regulatory risk level under FDA rules.
AI-generated from registry data and not verified by a human reviewer.
Information
- Country
- US
- Address
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- Website
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- Phone
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- PRRC Contact
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- EUDAMED SRN
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- FDA FEI Number
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- DUNS Number
- 480069957
Catalogue (2)
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Authorised Representatives
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Notified Bodies
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Authorities
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FDA Establishments (1)
Establishments registered with the FDA under this company group, matched by name.
- Oculocare Medical Ag Zurich · CH FEI 3016670763