Surgical Innovations Plc is one of 467 FDA 510(k) medical device manufacturers from United Kingdom in the dataset, ranked by real submission volume.
Surgical Innovations Plc - FDA 510(k) Cleared Devices
Recent clearances: PRETZELFLEX SURGICAL RETRACTOR MODEL SHR7301, SURGICAL RETRACTORS, LOGIC LAPAROSCOPIC INSTRUMENT SYSTEM
7
Total
7
Cleared
0
Denied
Surgical Innovations Plc has 7 FDA 510(k) cleared medical devices. Based in Leeds, GB.
Historical record: 7 cleared submissions from 1996 to 2013. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Surgical Innovations Plc Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Intertek Testing Services as regulatory consultant.
FDA 510(k) Regulatory Record - Surgical Innovations Plc
7 devices
Cleared
Jan 17, 2013
PRETZELFLEX SURGICAL RETRACTOR MODEL SHR7301
General & Plastic Surgery
106d
Cleared
Mar 09, 2012
SURGICAL RETRACTORS
General & Plastic Surgery
178d
Cleared
Jan 26, 2012
LOGIC LAPAROSCOPIC INSTRUMENT SYSTEM
General & Plastic Surgery
197d
Cleared
Jul 15, 2010
LOGIFLEX LAPAROSCOPIC BAND POSITIONING DEVICE
General & Plastic Surgery
182d
Cleared
Dec 01, 2006
LOGIC LAPAROSCOPIC SCISSORS
General & Plastic Surgery
14d
Cleared
Jan 09, 1997
NUMO NM-1000 AUTOMATIC CARBON-DIOXIDE FOR ENDOSCOPE
Obstetrics & Gynecology
412d
Cleared
Aug 28, 1996
PORTLAND TROCARS
General & Plastic Surgery
82d