Peters Surgical is one of 174 FDA 510(k) medical device manufacturers from France in the dataset, ranked by real submission volume.
Peters Surgical - FDA 510(k) Cleared Devices
Recent clearances: Monotime and Optime R, Peters Surgical ADVANTIME Absorbable Suture (ADVANTIME)
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.
510(k) submissions have been managed by Peter Surgical as regulatory consultant.
FDA 510(k) Regulatory Record - 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