Beiersdorf, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Beiersdorf, Inc. - FDA 510(k) Cleared Devices
Recent clearances: ANTI-EMBOLISM STOCKINGS, MODELS 71055-00000-02, 71057-00000-02, 71059-00000-02, 71064-00000-02 & 71065-00000-02, CURAD SCAR THERAPY, CUTINOVA CAVITY
45
Total
39
Cleared
0
Denied
Beiersdorf, Inc. has 39 FDA 510(k) cleared general & plastic surgery devices. Based in Mchenry, US.
Historical record: 39 cleared submissions from 1977 to 2009.
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 - Beiersdorf, Inc.
45 devices
Cleared
Dec 18, 2009
ANTI-EMBOLISM STOCKINGS, MODELS 71055-00000-02, 71057-00000-02,...
General Hospital
261d
Cleared
Jun 18, 2003
CURAD SCAR THERAPY
General & Plastic Surgery
191d
Cleared
Aug 14, 1995
CUTINOVA CAVITY
General & Plastic Surgery
74d
Cleared
Mar 15, 1995
CUTIPLAST STERIL
General & Plastic Surgery
245d
Cleared
Dec 02, 1994
CUTINOVA THIN WOUND DRESSING
General & Plastic Surgery
74d
Cleared
Oct 07, 1994
NORTA
Gastroenterology & Urology
318d
Cleared
Jul 29, 1994
COVERLET ADHESIVE DRESSING
General & Plastic Surgery
184d
Cleared
Feb 25, 1994
ELASTOPLAST HEAT PLASTER
Physical Medicine
476d
Cleared
Nov 15, 1993
CUTIFILM(R) FILM
General & Plastic Surgery
329d
Cleared
Sep 09, 1992
LUEKOFLEX SURGICAL TAPE
General & Plastic Surgery
61d
Cleared
Aug 10, 1992
ACRYLASTIC
General & Plastic Surgery
118d
Cleared
Aug 10, 1992
TRICOPLAST
General & Plastic Surgery
118d
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