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Inside MedSpa
Intelligence for Medical-Aesthetics Owners
FDA CLEAREDIntense Pulsed Light Therapy Device — Sanhe LEFIS Electronics Co., Ltd.2 weeks agoFDA CLEAREDLASEmaR 1500 — Eufoton S.R.L.4 weeks agoFDA CLEAREDBarbed PDO Suture — Sutura Medical Technology, Inc.2 weeks agoFDA CLEAREDVeineo System (00MEDRF4000TCUS 05CR45iT 06Pedal1St) — F Care Systems USA, LLC4 weeks agoFDA CLEAREDERBECRYO 2 Cryosurgical Unit and Accessories — Erbe Elektromedizin GmbH3 weeks agoFDA CLEAREDMILAN System — Lumenis Be, Ltd.4 weeks agoFDA CLEAREDLipocosm Harmonic System — Lipocosm, LLC3 weeks agoFDA CLEAREDCurrentBody Skin LED Multi Light Therapy Mask (MK-110D) — The Beauty Tech Group, Ltd.4 weeks agoFDA CLEAREDLumiGlam Laser System (SHE-LSP601-3) — Beijing Sano Laser S&T Development Co.,Ltd3 weeks ago
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Open data.

We do the work of turning messy official sources into clean, structured datasets — and we give them away. Use them in your own articles, tools, research, or models. All we ask is a credit and a link.

FDA Recalls & 510(k) Clearances

Every FDA recall and device clearance touching medical aesthetics, last ~180 days.

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Medical-Spa Regulation by State

Who can inject, supervision, medical-director, good-faith-exam, and ownership rules for all 50 states + DC.

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License & attribution

Free to use — commercially too — with attribution and a link back to insidemedspa.com on the page where you use it. Example credit: “Data via Inside MedSpa.” The data is provided as-is for information; it isn't legal or medical advice.

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