Esthetic Medical, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Esthetic Medical, Inc. - FDA 510(k) Cleared Devices
Recent clearances: SkinStylus SteriLock MicroSystem (MP1209SL), SkinStylus SteriLock® MicroSystem, Model Number MP1209SL
2
Total
2
Cleared
0
Denied
Esthetic Medical, Inc. has 2 FDA 510(k) cleared medical devices. Based in Long Beach, US.
Latest FDA clearance: Feb 2026. Active since 2023. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Esthetic Medical, Inc. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Contract In-House Counsel and Consultants, as regulatory consultant. 1 device has linked clinical trial registered on ClinicalTrials.gov.
FDA 510(k) Regulatory Record - Esthetic Medical, Inc.
2 devices