Westaim Biomedical, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Westaim Biomedical, Inc. - FDA 510(k) Cleared Devices
6
Total
6
Cleared
0
Denied
Westaim Biomedical, Inc. has 6 FDA 510(k) cleared medical devices. Based in Exeter, US.
Historical record: 6 cleared submissions from 1998 to 2001. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Westaim Biomedical, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Westaim Biomedical, Inc.
6 devices
Cleared
Mar 15, 2001
MODIFICATION TO ACTICOAT FOAM DRESSING
General & Plastic Surgery
30d
Cleared
Feb 16, 2001
ACTICOAT COMPOSITE DRESSING
General & Plastic Surgery
189d
Cleared
Oct 06, 2000
ACTICOAT 7 DRESSING
General & Plastic Surgery
143d
Cleared
Jun 07, 2000
ACTICOAT PRIMARY ANTIMICROBIAL DRESSING
General & Plastic Surgery
342d
Cleared
Apr 05, 2000
ACTICOAT FOAM DRESSING
General & Plastic Surgery
89d
Cleared
Dec 10, 1998
ACTICOAT COMPOSITE WOUND DRESSING, ACTICOAT COMPOSITE WOUND DRESSING-ADHESIVE
General & Plastic Surgery
41d