Medical Device Manufacturer · US , Reno , NV

Carl Zeiss Meditec Cataract Technology, Inc. - FDA 510(k) Cleared Dev...

7 submissions · 7 cleared · Since 2019
7
Total
7
Cleared
0
Denied

Carl Zeiss Meditec Cataract Technology, Inc. has 7 FDA 510(k) cleared medical devices. Based in Reno, US.

Latest FDA clearance: Aug 2025. Active since 2019. Primary specialty: Ophthalmic.

Browse the FDA 510(k) cleared devices submitted by Carl Zeiss Meditec Cataract Technology, Inc. Filter by specialty or product code using the sidebar.

Regulatory submissions have been managed by GSM Services and GSM Services, Inc..

FDA 510(k) Regulatory Record - Carl Zeiss Meditec Cataract Technology, Inc.
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