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Optomedical Technologies GmbH

GermanyFDA applicant, unverified

Devices
2

What Optomedical Technologies GmbH makes

Optomedical Technologies GmbH manufactures OCT-Camera devices, including the OCT-Camera ID 21101A3, which are optical coherence tomography cameras used for medical imaging.

The company's devices are classified as Class II and are listed in the FDA 510(k) registry. Optomedical Technologies GmbH is based in the US.

AI-generated from registry data, 3 Oct 2026. Not verified by deviCERTS or the manufacturer.

Catalogue2

Newest first, rows 1-2 of 2

  • OCT-Camera Ref K142953 Open recall

    Active Regimes: 510(k) Registry: 510(k) Class:II
  • OCT-Camera ID 21101A3 Ref K200516

    Active Regimes: 510(k) Registry: 510(k) Class:II

Frequently asked questions

How many devices does Optomedical Technologies GmbH have in the registry?

The registry currently lists 2 devices for Optomedical Technologies GmbH. Devices recorded under merged duplicate company entries are counted once.

Which registries list Optomedical Technologies GmbH's devices?

Among its 2 most recently registered devices, Optomedical Technologies GmbH has devices listed in FDA 510(k) (2 devices).

What risk classes do Optomedical Technologies GmbH's devices fall under?

Among its 2 most recently registered devices, the classes recorded for Optomedical Technologies GmbH's devices are Class II. Each device page shows its own class and authorisation.

What are the newest devices from Optomedical Technologies GmbH in the registry?

The most recently registered devices listed for Optomedical Technologies GmbH include OCT-Camera and OCT-Camera ID 21101A3.

Generated automatically from registry data and not verified by a human reviewer.