Conmedcorp is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Conmedcorp - FDA 510(k) Cleared Devices
Recent clearances: CONMED ALTRUS THERMAL TISSUE FUSION SYSTEM, ENTAKE STANDARD AND SAFETY PEG SYSTEM, CONMED IRRIGATION NOZZLE
92
Total
92
Cleared
0
Denied
Conmedcorp has 92 FDA 510(k) cleared medical devices. Based in Dayton, US.
Historical record: 92 cleared submissions from 1981 to 2010. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Conmedcorp 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 - Conmedcorp
92 devices
Cleared
Nov 24, 2010
CONMED ALTRUS THERMAL TISSUE FUSION SYSTEM
General & Plastic Surgery
174d
Cleared
Apr 28, 2006
ENTAKE STANDARD AND SAFETY PEG SYSTEM
Gastroenterology & Urology
15d
Cleared
Jul 14, 2005
CONMED IRRIGATION NOZZLE
Gastroenterology & Urology
86d
Cleared
Apr 22, 2005
PROFORMA HF 4.5 CANNULA, MODEL 050906, 050907
Gastroenterology & Urology
25d
Cleared
Mar 08, 2005
FX WIRE ADVANCED MEASUREMENT GUIDEWIRE
Gastroenterology & Urology
28d
Cleared
Aug 09, 2004
VERSASTIM, PERFOAMAX, SURGI-STIM, FASTSTART
Neurology
20d
Cleared
Jul 01, 2002
ABCSNARE ELECTROSURGICAL PROBE FOR FLEXIBLE ENDOSCOPES, MODEL 1336XX
General & Plastic Surgery
89d
Cleared
Jun 26, 2002
CONMED HEATWAVE HAND-CONTROLLED ELETRODE
General & Plastic Surgery
63d
Cleared
Apr 12, 2002
CONMED SYSTEM 2000 ELECTROSURGICAL GENERATOR, REF: 60-8002
General & Plastic Surgery
87d
Cleared
Apr 12, 2002
CONMED SYSTEM 5000 ESU
General & Plastic Surgery
84d
Cleared
Aug 17, 2000
SUREFIT DISPERSIVE ELECTRODE
General & Plastic Surgery
48d
Cleared
Jun 07, 2000
HYFRECATOR 2000 REUSABLE HAND-SWITCHING ACCESSORY HANDPIECE/FOOT-SWITCHING...
General & Plastic Surgery
58d
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