EvidenceOS Hub

Regulatory Clearances

FDA 510(k) clearance records for the underlying ActiPatch and RecoveryRx devices.

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Answers come only from verified EvidenceOS sources and curated Electrome / ActiPatch public facts.

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Educational summary only. Not medical advice. Individual results vary. Consult a qualified healthcare provider before making treatment decisions.

ActiPatch® is FDA-cleared under 510(k) K192234 for over-the-counter (OTC) adjunctive treatment of musculoskeletal pain. FDA 510(k) clearance is not the same as FDA approval (PMA), and should not be inferred to cover every study outcome summarized on this page.