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
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.
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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