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Mps Medical, Inc.

FDA Regulatory Profile

Mps Medical, Inc. has 0 FDA recalls, 3 inspections, 1 510(k) clearance and 0 compliance actions on record.

Latest inspection
Aug 5, 2022 · NAI
Latest 510(k)
Jul 30, 2020

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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
Inspections3Oct 25, 2026Not statedCurrent
Compliance actions0Oct 23, 2026Not statedCurrent

Recent FDA Inspections

DateSiteProductClassificationFEI
Aug 5, 2022Brea, CADevicesNo Action Indicated (NAI)3011183328
Apr 7, 2021Brea, CADevicesNo Action Indicated (NAI)3011183328
Mar 16, 2018Brea, CADevicesVoluntary Action Indicated (VAI)3011183328

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
K200082BD Univia RightFit Enteral Extension Sets and Transitional AdaptersJul 30, 2020

FDA data resources