Peters Surgical - FDA 510(k) Cleared Devices
7
Total
7
Cleared
0
Denied
Peters Surgical has 7 FDA 510(k) cleared medical devices. Based in Bobigny, FR.
Latest FDA clearance: Oct 2024. Active since 2005. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Peters Surgical Filter by specialty or product code using the sidebar.
FDA 510(k) cleared devices by Peters Surgical
7 devices
Cleared
Oct 11, 2024
Monotime and Optime R
General & Plastic Surgery
378d
Cleared
Jul 12, 2024
Peters Surgical ADVANTIME Absorbable Suture (ADVANTIME)
General & Plastic Surgery
339d
Cleared
Aug 03, 2007
UNIRING - ANNULOPLASTY RING WITH SIZERS
Cardiovascular
88d
Cleared
Jan 17, 2007
PREMIO
General & Plastic Surgery
329d
Cleared
Oct 11, 2006
CARDIOFLON, CARDIOXYL
General & Plastic Surgery
261d
Cleared
Oct 02, 2006
OPTIME, SINUSORB PGA
General & Plastic Surgery
49d
Cleared
Dec 13, 2005
COROLENE
General & Plastic Surgery
76d