Tissue Science Laboratories, Plc is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Tissue Science Laboratories, Plc - FDA 510(k) Cleared Devices
6
Total
6
Cleared
0
Denied
Tissue Science Laboratories, Plc has 6 FDA 510(k) cleared medical devices. Based in Washington, US.
Historical record: 6 cleared submissions from 2000 to 2006. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Tissue Science Laboratories, Plc Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Tissue Science Laboratories, Plc
6 devices
Cleared
Jun 23, 2006
ZIMMER COLLAGEN REPAIR PATCH
General & Plastic Surgery
184d
Cleared
Mar 09, 2005
PERMACOL SURGICAL IMPLANT T-PIECE, PERMACOL SURGICAL IMPLANT RECTOCELE-PIECE,...
Obstetrics & Gynecology
23d
Cleared
Dec 17, 2004
PERMACOL SURGICAL IMPLANT
General & Plastic Surgery
9d
Cleared
Oct 31, 2002
PERMACOL
General & Plastic Surgery
213d
Cleared
Jan 17, 2002
PERMACOL
General & Plastic Surgery
73d
Cleared
Feb 17, 2000
PERMACOL
General & Plastic Surgery
202d