Conmedcorp

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
92
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K101534CONMED ALTRUS THERMAL TISSUE FUSION SYSTEMNovember 24, 2010
K061021ENTAKE STANDARD AND SAFETY PEG SYSTEMApril 28, 2006
K050992CONMED IRRIGATION NOZZLEJuly 14, 2005
K050777PROFORMA HF 4.5 CANNULA, MODEL 050906, 050907April 22, 2005
K050304FX WIRE ADVANCED MEASUREMENT GUIDEWIREMarch 8, 2005
K041953VERSASTIM, PERFOAMAX, SURGI-STIM, FASTSTARTAugust 9, 2004
K021079ABCSNARE ELECTROSURGICAL PROBE FOR FLEXIBLE ENDOSCOPES, MODEL 1336XXJuly 1, 2002
K021299CONMED HEATWAVE HAND-CONTROLLED ELETRODEJune 26, 2002
K020135CONMED SYSTEM 2000 ELECTROSURGICAL GENERATOR, REF: 60-8002; CONMED ESU CART, REF: 60-6120April 12, 2002
K020186CONMED SYSTEM 5000 ESUApril 12, 2002
K002002SUREFIT DISPERSIVE ELECTRODEAugust 17, 2000
K001161ULTRAPEN REUSABLE PENCIL, MODEL 130350 THROUGH 130353, REUSABLE ACCESSORY ELECTRODE KIT (FOR USE WITJune 7, 2000
K001159HYFRECATOR 2000 REUSABLE HAND-SWITCHING ACCESSORY HANDPIECE/FOOT-SWITCHING ACCESSORY HANDPIECE, HYFRJune 7, 2000
K001597CONMED TROGARD FINESSE TROCAR SYSTEM, MODEL 60-6050-XXXJune 5, 2000
K991105ECG ELECTRODE (VARIOUS)November 26, 1999
K992186QUAD BIPOLAR LAPAROSCOPIC COAGULATING AND CUTTING INSTRUMENTJuly 30, 1999
K991855CONMED STEALTH NON-STICK ACCESSORY ELECTRODE, MODEL 138XXXJune 15, 1999
K990586CONMED ABC PROBE FOR FLEXIBLE ENDOSCOPESMay 17, 1999
K983782ELECTROSURGICAL DISPERSIVE ELECTRODEJanuary 25, 1999
K982309SMOKE EVACUATION ATTACHMENT 130XXX TBDAugust 5, 1998