Pegasus Biologics, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Pegasus Biologics, Inc. - FDA 510(k) Cleared Devices
5
Total
5
Cleared
0
Denied
Pegasus Biologics, Inc. has 5 FDA 510(k) cleared medical devices. Based in Irvine, US.
Historical record: 5 cleared submissions from 2005 to 2009. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Pegasus Biologics, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Pegasus Biologics, Inc.
5 devices
Cleared
May 05, 2009
ORTHADAPT PR
General & Plastic Surgery
89d
Cleared
Jun 20, 2007
UNITE BIOMATRIX
General & Plastic Surgery
28d
Cleared
May 04, 2007
ORTHADAPT BIOIMPLANT
General & Plastic Surgery
18d
Cleared
Sep 21, 2006
DERMADAPT WOUND DRESSING
General & Plastic Surgery
113d
Cleared
Aug 05, 2005
PEGASUS BIOLOGICS ORTHADAPT SURGICAL MESH
General & Plastic Surgery
239d