Synergetics, Inc. - FDA 510(k) Cleared Devices
16
Total
16
Cleared
0
Denied
Synergetics, Inc. has 16 FDA 510(k) cleared medical devices. Based in Chesterfield, US.
Historical record: 16 cleared submissions from 1992 to 2012.
Browse the FDA 510(k) cleared devices submitted by Synergetics, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) cleared devices by Synergetics, Inc.
16 devices
Cleared
Jul 10, 2012
AYNERGETICS DISPOSABLE SPETZLER-MALIS STANDARD BIPOLAR FORCEPS
General & Plastic Surgery
57d
Cleared
Jun 21, 2012
VERSAVIT
Ophthalmic
15d
Cleared
Apr 23, 2012
SYNERGETICS DIRECTIONAL ENDOOCULAR LASER PROBE
Ophthalmic
115d
Cleared
Dec 07, 2011
DISPOSABLE SPETZLER-MALIS DUAL IRRIGATING BIPOLAR FORCEPS
General & Plastic Surgery
247d
Cleared
Oct 30, 2009
SYNERGETICS ADJUSTABLE GAS PRESSURIZED INFUSION (AGPI) TUBE SET
General Hospital
168d
Cleared
Dec 20, 2007
STRYKER RF MULTI-LESION GENERATOR, MODEL 0406-900-000
Neurology
204d
Cleared
May 23, 2007
STRYKER INTRADISCAL RF GENERATOR
Neurology
187d
Cleared
Nov 24, 2003
SYNERGETICS SYNERLIGHT FIBER OPTIC LIGHTSOURCE
Ophthalmic
91d
Cleared
Aug 23, 2002
ULTRASONIC STRAIGHT/ULTRASONIC KNIFE/ULTRASONIC RING CURRETTE
General & Plastic Surgery
213d
Cleared
Apr 20, 2001
SONOTOME ULTRASONIC ASPIRATOR TIPS
General & Plastic Surgery
46d
Cleared
May 14, 1999
SCRAMBLED ENDOOTO LASER PROBE, STRAIGHT TIP, MODEL 59.02, SCRAMBLED ENDOOTO...
General & Plastic Surgery
80d
Cleared
Dec 02, 1998
VERITAS BIPOLAR, INSULATED, 0.5MM TIP, MODEL N301-005 VERITAS BIPOLAR,...
General & Plastic Surgery
162d