Berchtold Holding GmbH is one of 237 FDA 510(k) medical device manufacturers from Germany in the dataset, ranked by real submission volume.
Berchtold Holding GmbH - FDA 510(k) Cleared Devices
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
Cleared
Oct 30, 2008
CHROMOPHARE E 778 AND E 558
General & Plastic Surgery
15d
Cleared
Apr 10, 2008
CHROMOPHARE E-SERIES
General & Plastic Surgery
14d
Cleared
Mar 21, 2003
CHROMOPHARE X 65
General & Plastic Surgery
95d
Cleared
Jul 20, 1999
CHROMOPHARE D 530 LDR SURGICAL LIGHT
General & Plastic Surgery
141d
Cleared
May 27, 1999
CHROMOPHARE D500, D530, D650
General & Plastic Surgery
24d
Cleared
Feb 20, 1998
CHROMOPHARE D 500, CHROMOPHARE D 530
General & Plastic Surgery
88d
Cleared
Jul 14, 1997
CHROMOPHARE
General & Plastic Surgery
203d
Cleared
Feb 08, 1996
TELETOM
General & Plastic Surgery
52d
Cleared
Mar 15, 1995
BIPOLAP HOOK ELECTRODE
General & Plastic Surgery
14d
Cleared
Oct 19, 1994
CHROMOPHARE
General & Plastic Surgery
19d
Cleared
Jun 08, 1994
HIRSCH BIPOLAR COAGULATION FORCEPS AND ADAPTOR CABLES
General & Plastic Surgery
26d
Cleared
Apr 14, 1994
TELETOM
General Hospital
77d