Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

Enovis

FDA 510(k) & PMA Approved Devices — 1 products

Total Devices1
Categories1
Latest FDA decision2025-01-17

SEC Filings: 1 filings on record. Latest: 8-K (2026-08-06). View on SEC EDGAR →

TypeNumberDevice NameCodeDateActions
PMA P210016 Stimulator, bone growth, non-invasiveLOF2025-01-17 View

Related Clinical Trials

NCT06759935Performance and Safety of LightForce® Therapy Lasers on Shoulder Soft Tissue Inflammation Pain ReductionCOMPLETEDNCT06854016Performance and Safety of LightForce® Therapy Lasers on Lateral Ankle SprainCOMPLETED
↑