Prosurg, Inc. - FDA 510(k) Cleared Devices
16
Total
16
Cleared
0
Denied
Prosurg, Inc. has 16 FDA 510(k) cleared medical devices. Based in San Jose, US.
Historical record: 16 cleared submissions from 2000 to 2016.
Browse the FDA 510(k) cleared devices submitted by Prosurg, Inc. Filter by specialty or product code using the sidebar.
16 devices
Cleared
Jul 11, 2016
Neo - Arthroscope (Rigid) 2.0mm/3.5mm, Outer sheath/ cannula, Outer sheath/...
Orthopedic
313d
Cleared
May 19, 2016
Neo-Bronchoscope -Digital Video Bronchoscopy System(Rigid/Flexible)
Ear, Nose, Throat
262d
Cleared
Apr 29, 2016
Neoscope 3D - 3D Digital Video Endoscopic System (Rigid/Flexible)
General & Plastic Surgery
228d
Cleared
Sep 11, 2012
ENDOSCOPIC DIAGNOSTIC & TREATMENT SYSTEM (MODIFICATION)
Gastroenterology & Urology
182d
Cleared
Dec 28, 2007
ADJUSTABLE BONE PLATES BIOABSORBABLE, SELF COMPRESSION BONE FIXATION SYSTEM &...
Dental
112d
Cleared
Aug 15, 2007
CRANIOCLAMP BIOABSORBABLE CRANIAL BONE FLAP FIXATION SYSTEM
Neurology
152d
Cleared
Jul 25, 2007
XSORB BIOABSORBABLE CRANIOFACIAL BONE FIXATION SYSTEM & ACCESSORIES
Dental
131d
Cleared
Jul 02, 2007
MINISLING ADJUSTABLE POLYMER SLING & SURGICAL MESH WITH SELF-ANCHORING SYSTEM
General & Plastic Surgery
96d
Cleared
Apr 05, 2006
LASERTX - DIODE LASER & DELIVERY SYSTEM
General & Plastic Surgery
55d
Cleared
Apr 01, 2005
TURBT-RF ELECTRODES AND ELECTROSURGICAL DEVICES
Gastroenterology & Urology
35d
Cleared
Feb 03, 2005
NEOSCOPE - ENDOSCOPIC DIAGNOSTIC & TREATMENT SYSTEM
Gastroenterology & Urology
120d
Cleared
May 19, 2003
ZIPPERE - BIOABSORBABLE/NON-ABSORBABLE POLYMER SLING & SURGICAL MESH
General & Plastic Surgery
80d