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BEAR

Model 1.04.15 · Bear-Ent, LLC · DI G043104150

KAM — Cannula, Sinus · Class I · 21 CFR 878.4800

UDILibrary device dossier · generated 2026-09-14 · 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 — Bear-Ent, LLC

  • VAI 2026-02-26 Bear-Ent, Llc · 7 citations
  • VAI 2026-02-26 Bear-Ent, Llc · 7 citations