Coloplast Corp. - FDA 510(k) Cleared Devices
54
Total
47
Cleared
0
Denied
FDA 510(k) cleared devices by Coloplast Corp. General & Plastic Surgery ✕
20 devices
Cleared
Mar 22, 2024
Biatain Fiber Ag (33570 - 5 cm x 5 cm / 2 in x 2 in)
General & Plastic Surgery
266d
Cleared
Dec 10, 2018
SabreLine and SabreGuard Laser Fibers
General & Plastic Surgery
62d
Cleared
May 17, 2004
CONTREET FOAM CAVITY DRESSING WITH SILVER, MODEL 9628 (2X4 IN.)
General & Plastic Surgery
157d
Cleared
Feb 03, 2003
CONTREET FOAM ADHESIVE/NON-ADHESIVE
General & Plastic Surgery
194d
Cleared
Oct 04, 2002
CONTREET-H ANTIMICROBIAL HYDROCOLLOID DRESSING, MODELS 9610 (4 X 4 (10 CM X...
General & Plastic Surgery
346d
Cleared
Jun 04, 1999
MODIFICATION TO WOUN'DRES
General & Plastic Surgery
74d
Cleared
Jan 28, 1999
COMPEED PSORIASIS DRESSING
General & Plastic Surgery
195d
Cleared
Dec 30, 1998
COMFEEL SEASORB DRESSING
General & Plastic Surgery
83d
Cleared
Dec 16, 1998
BIATAIN FOAM DRESSING
General & Plastic Surgery
97d
Cleared
Dec 16, 1998
BIATAIN FOAM ADHESIVE DRESSING
General & Plastic Surgery
97d
Cleared
Nov 25, 1998
SWEEN WOUN'DRES
General & Plastic Surgery
86d
Cleared
Jul 29, 1997
COMFEEL PURILON GEL,15G(3900)/COMFEEL PURILON GEL,25G(3903)
General & Plastic Surgery
89d