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Rehabtronics, Inc.

FDA Regulatory Profile

Rehabtronics, Inc. has 0 FDA recalls, 3 inspections, 2 510(k) clearances and 1 compliance action on record.

Latest inspection
Jul 13, 2023 · VAI
Latest 510(k)
May 13, 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) clearances2Oct 4, 2026Not statedCurrent
Inspections3Oct 26, 2026Not statedCurrent
Compliance actions1Oct 23, 2026Not statedCurrent

Recent FDA Inspections

DateSiteProductClassificationFEI
Jul 13, 2023Edmonton, CanadaDevicesVoluntary Action Indicated (VAI)3007999109
Feb 26, 2015Edmonton, CanadaDevicesVoluntary Action Indicated (VAI)3007999109
Aug 8, 2013Edmonton, CanadaDevicesOfficial Action Indicated (OAI)3007999109

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
K210979PreliviaMay 13, 2021
K153163ReGraspApr 7, 2016

FDA data resources