Medical Device Manufacturer · DE , Tuttlingen

Berchtold Holding GmbH - FDA 510(k) Cleared Devices

16 submissions · 16 cleared · Since 1992

Recent clearances: CHROMOPHARE E 778 AND E 558, CHROMOPHARE E-SERIES, CHROMOPHARE X 65

16
Total
16
Cleared
0
Denied

Berchtold Holding GmbH has 16 FDA 510(k) cleared general & plastic surgery devices. Based in Tuttlingen, DE.

Historical record: 16 cleared submissions from 1992 to 2008.

Browse the complete list of FDA 510(k) cleared general & plastic surgery devices from this manufacturer. Filter by specialty or product code using the sidebar.

510(k) submissions have been managed by Underwriters Laboratories, Inc. as regulatory consultant.

FDA 510(k) Regulatory Record - Berchtold Holding GmbH

16 devices
1-12 of 16
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