Beiersdorf-Jobt, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Beiersdorf-Jobt, Inc. - FDA 510(k) Cleared Devices
5
Total
5
Cleared
0
Denied
Beiersdorf-Jobt, Inc. has 5 FDA 510(k) cleared medical devices. Based in Charlotte, US.
Historical record: 5 cleared submissions from 1999 to 1999. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Beiersdorf-Jobt, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Beiersdorf-Jobt, Inc.
5 devices
Cleared
Aug 20, 1999
JOBST READY-TO-WEAR ARM SLEEVES
General Hospital
107d
Cleared
Mar 01, 1999
MODIFICATION OF CUTINOVA THIN DRESSING
General & Plastic Surgery
63d
Cleared
Mar 01, 1999
MODIFICATION OF CUTINOVA HYDRO DRESSING
General & Plastic Surgery
63d
Cleared
Mar 01, 1999
MODIFICATION OF CUTINOVA CAVITY DRESSING
General & Plastic Surgery
63d
Cleared
Mar 01, 1999
MODIFICATION OF CUTINOVA FOAM DRESSING
General & Plastic Surgery
63d