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MicroFrance®

INTEGRA MICROFRANCE · Model CP333 · UDI-DI 10381780098782

KAD Prescription
5
510(k) clearances
21
Adverse events
1
Recalls
120
Facilities

Description

KNIFE CP333 160MM ANG JOSEPH

Recalls

DateFirmReason
2024-12-03Sklar InstrumentsReports of various packaging issues that may result in a breach of the sterile barrier.

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Linked GUDID · 510(k)/PMA · MAUDE · recalls · establishments. Free tier, no card required.

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Data compiled from public U.S. FDA sources (GUDID, 510(k)/PMA, MAUDE, recalls, establishment registration). Adverse-event reports are unverified and do not establish causation. Informational only — not medical, clinical, or regulatory advice.