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Integra Microfrance

FDA Regulatory Profile

Integra Microfrance has 0 FDA recalls, 2 inspections, 1 510(k) clearance and 0 compliance actions on record.

Latest inspection
Feb 18, 2016 · NAI
Latest 510(k)
May 14, 2021

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Summary

Record counts and when each FDA source was last refreshed
RecordsCountLast refreshedSource as ofStatus
Recalls0Oct 23, 2026Not statedCurrent
510(k) clearances1Oct 4, 2026Not statedCurrent
Inspections2Oct 26, 2026Not statedCurrent
Compliance actions0Oct 23, 2026Not statedCurrent

Recent FDA Inspections

DateSiteProductClassificationFEI
Feb 18, 2016St Aubin Le Monial, FranceDevicesNo Action Indicated (NAI)3003249645
Sep 12, 2013St Aubin Le Monial, FranceDevicesVoluntary Action Indicated (VAI)3003249645

NAI means no objectionable conditions or practices were found during the inspection. VAI means objectionable conditions or practices were found, but the agency is not prepared to take or recommend any administrative or regulatory action. OAI means regulatory and/or administrative actions are recommended.

Recent 510(k) Clearances

K-NumberDeviceDate
K210942MicroFrance Monopolar and Bipolar Electrosurgical InstrumentsMay 14, 2021

FDA data resources