Medical Device Manufacturer · DE , Luebeck

Optomedical Technologies GmbH - FDA 510(k) Cleared Devices

2 submissions · 2 cleared · Since 2015

Recent clearances: OCT-Camera ID 21101A3

2
Total
2
Cleared
0
Denied

Optomedical Technologies GmbH has 2 FDA 510(k) cleared medical devices. Based in Luebeck, DE.

Historical record: 2 cleared submissions from 2015 to 2020. Primary specialty: Ophthalmic.

Browse the FDA 510(k) cleared devices submitted by Optomedical Technologies GmbH Filter by specialty or product code using the sidebar.

510(k) submissions have been managed by Emergo Global Consulting, LLC as regulatory consultant.

FDA 510(k) Regulatory Record - Optomedical Technologies GmbH

2 devices
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