Boston Aesthetics, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Boston Aesthetics, Inc. - FDA 510(k) Cleared Devices
Recent clearances: Boston 2910 (Boston 2910), Boston PICO (Boston PICO), Boston Pico755
6
Total
6
Cleared
0
Denied
Boston Aesthetics, Inc. has 6 FDA 510(k) cleared medical devices. Based in Wilmington, US.
Latest FDA clearance: May 2026. Active since 2025. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Boston Aesthetics, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Boston Aesthetics, Inc.
6 devices
Cleared
May 21, 2026
Boston 2910 (Boston 2910)
General & Plastic Surgery
234d
Cleared
Jan 30, 2026
Boston PICO (Boston PICO)
General & Plastic Surgery
217d
Cleared
Jan 21, 2026
Boston Pico755
General & Plastic Surgery
175d
Cleared
Jan 12, 2026
Boston iFace (Boston iFace)
General & Plastic Surgery
199d
Cleared
Mar 13, 2025
308nm UV Phototherapy System (UV-K)
General & Plastic Surgery
76d
Cleared
Feb 13, 2025
Unicorn+ RF System (Unicorn+)
General & Plastic Surgery
233d