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Eva Medtec, Inc.

FDA Regulatory Profile

Eva Medtec, Inc. has 0 FDA recalls, 2 inspections, 1 510(k) clearance and 0 compliance actions on record.

Latest inspection
May 6, 2026 · NAI
Latest 510(k)
Mar 5, 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
May 6, 2026Shakopee, MNDevicesNo Action Indicated (NAI)3018383120
Aug 17, 2022Shakopee, MNDevicesNo Action Indicated (NAI)3018383120

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
K202693NeoWave Pain Relief and Recovery System, Model# T16-2020Mar 5, 2021

FDA data resources