FDA Device Intelligence
HomeINTEGRA MICROFRANCE › MicroFrance®

MicroFrance®

INTEGRA MICROFRANCE · Model MCOS21 · UDI-DI 10381780111368

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

Description

MicroFrance® Selesnick curved elevator, 190 mm

Recalls

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

Query this across every FDA database — by API.

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

Get your free API keyRead the docs
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.