Berchtold Holding GmbH is one of 234 FDA 510(k) medical device manufacturers from Germany in the dataset, ranked by real submission volume.
Berchtold Holding GmbH - FDA 510(k) Cleared Devices
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.
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
Cleared
Feb 03, 1994
CHROMOPHARE
General Hospital
58d
Cleared
Oct 09, 1992
CHROMOPHARE
General & Plastic Surgery
119d
Cleared
Jul 23, 1992
BICUT
General & Plastic Surgery
220d
Cleared
May 05, 1992
TELETOM(R)
General & Plastic Surgery
29d