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Conmed Corporation

1626 adverse events · 282 recalls · 71 clearances · 40 inspections · 2 compliance actions · aggregated across 4 source records

Scorecard
Events per device across the 7,552-device portfolio, trailing 12 months. Arrows compare the last 90 days with the 90 before.

MAUDE reports per device

0.061

459 in the last 12 months

Higher volume than 92% of companies with 10+ devices

Recalls per device

0.003

22 in the last 12 months

Higher volume than 98% of companies with 10+ devices

These are reporting-volume percentiles, not safety rankings — MAUDE counts have no denominator of devices in use, and recall attribution follows resolved links. A high percentile means more reports per registered device than peers, which can reflect market size, device criticality, or reporting practice as much as anything else.

Devices
7,552 device records · ordered by linked event volume.
BrandModelProduct codesPrimary DILinked events
VCARE60-6085-201ALKF10653405003793485
CONMEDAES-90SNGEI10653405006473154
AIRSEALAS-iFS1HIF10851885004587133
VCARE60-6085-202ALKF10653405003809123
VCARE60-6085-200ALKF10653405003748107
CONMED138104GEI30653405003391105
PlumePenPLPUL2020GEI2084585406121084
AIRSEALIAS12-100LPIGCJ1084585404564083
PlumePenPLP2020GEI1084585406128272
CONMED GOLDLINE138114AGEI3065340505629865
ANCHOR TISSUE RETRIEVAL SYSTEMTRS100SB2GCJ2065340598610956
CleanGuideDIS150OCY1065340598655354
UltraClean139112EXTGEI4065340503477446
CORE DYNAMICSCD801GCJ2065340504327745
AIRSEALAS-iFS1HIF3085188500458144
CONMED138110GEI3065340500345242
UNIVERSAL PLUS60-5274-132GEI3065340501073337
AIRSEALIAS8-120LPGCJ1084585404570136
CONMEDAES-50SLGEI1065340500497435
ANCHOR TISSUE RETRIEVAL SYSTEMTRS-ROBO-8GCJ2065340598614734
AIRSEALIAS12-120LPIGCJ1084585404568833
CONMED GOLDLINE130309AGEI3065340505615133
Y-KNOTY1301MBI2084585402165832
PlumePenPLP2520GEI1084585406130526
CONMED00507118100GFA1084585400908625
HallPRO7000DEHAB1084585404090425
AIRSEALASM-EVAC1HIF1084585404543524
ANCHOR TISSUE RETRIEVAL SYSTEMTRS175SB2GCJ2065340598611624
LAPAROVUELAPVUE10GCJ2084585406174624
ProPLP2020GEI2084585406128924
Showing 1–30 of 7,552Next →
Compliance actions
FDA warning letters and enforcement actions (full history).
DateTypeActionFirm
2014-01-29WLWarning LetterConMed Corporation
2014-01-29WLWarning LetterConMed Corporation
Facilities
Registered establishments with their latest FDA inspection outcome.
FEINameLocationLast inspectionWatch
3001451571CONMED CORPORATIONUtica, NY, USNAI
3004491689ConMed CorporationGreenwood Village, CO, USVAI
3019101334ConMed CorporationNew Haven, CT, USNAI
1000305720Conmed CorporationWESTBOROUGH, MA, USNAI
3007305485Consolidated Medical Equipment CompanyChihuahua, MX
1017294Linvatec CorporationLARGO, FL, USNAI