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AER DEFENSE

Conmed Corporation

UDILibrary device dossier · generated 2026-09-10 · sources: FDA GUDID, openFDA (recalls, MAUDE, 510(k)/PMA), FDA Data Dashboard (inspections, compliance actions), 510(k) summary documents.

Recall history (0)

No recalls linked in the loaded window.

Adverse-event reports — MAUDE (0)

Caveat (required reading): MAUDE report counts cannot be used to compute incidence rates or compare device safety. Reporting is incomplete, duplicated, and spikes with publicity; there is no denominator of devices in use. The peer line is a reporting baseline (average device in the same product code), not a risk measure.

No dated reports to chart.

Regulatory clearances

  • None linked in the loaded window.

Manufacturer compliance record — Conmed Corporation

  • Warning Letter 2014-01-29 ConMed Corporation
  • Warning Letter 2014-01-29 ConMed Corporation
  • NAI 2026-05-13 Biorez, Inc · 0 citations
  • VAI 2026-04-06 ConMed Corporation · 6 citations
  • VAI 2026-04-06 ConMed Corporation · 6 citations
  • NAI 2023-12-14 Linvatec Corp. · 0 citations
  • VAI 2023-08-04 Biorez, Inc · 1 citations
  • NAI 2022-11-10 ConMed Corporation · 0 citations
  • NAI 2022-11-10 ConMed Corporation · 0 citations
  • NAI 2022-07-13 ConMed Corporation · 0 citations
  • NAI 2022-07-13 ConMed Corporation · 0 citations
  • VAI 2020-09-22 ConMed Corporation · 0 citations
  • VAI 2020-09-22 ConMed Corporation · 0 citations
  • NAI 2019-10-17 ConMed Corporation · 0 citations
  • NAI 2019-10-17 ConMed Corporation · 0 citations
  • VAI 2017-02-03 ConMed Corporation · 2 citations
  • VAI 2017-02-03 ConMed Corporation · 2 citations
  • NAI 2017-01-23 Conmed · 0 citations
  • VAI 2016-02-03 ConMed Corporation · 5 citations
  • VAI 2016-02-03 ConMed Corporation · 5 citations
  • NAI 2014-11-18 ConMed Corporation · 0 citations
  • NAI 2014-11-18 ConMed Corporation · 0 citations