Foreo, Inc. - FDA 510(k) Cleared Devices
10
Total
10
Cleared
0
Denied
Foreo, Inc. has 10 FDA 510(k) cleared general & plastic surgery devices. Based in Las Vegas, US.
Latest FDA clearance: Feb 2026. Active since 2016.
Browse the complete list of FDA 510(k) cleared general & plastic surgery devices from this manufacturer. Filter by specialty or product code using the sidebar.
FDA 510(k) cleared devices by Foreo, Inc.
10 devices
Cleared
Feb 20, 2026
FAQ™ (LED Panel)
General & Plastic Surgery
91d
Cleared
Dec 11, 2024
FAQ™ (302)
General & Plastic Surgery
90d
Cleared
Aug 20, 2024
Luna 4 plus
General & Plastic Surgery
120d
Cleared
Jul 15, 2024
FAQ™ (102)
Physical Medicine
132d
Cleared
May 13, 2024
BEAR 2 Body
Neurology
290d
Cleared
Apr 19, 2024
FAQ™ 201, FAQ™ 202
General & Plastic Surgery
72d
Cleared
Sep 25, 2023
PEACH 2, PEACH 2 Duo, PEACH 2 go
General & Plastic Surgery
84d
Cleared
Apr 05, 2023
FAQ 101
General & Plastic Surgery
271d
Cleared
Jul 31, 2020
BEAR and BEAR mini
Neurology
126d
Cleared
Nov 30, 2016
ESPADA Acne-Clearing Blue Light Pen
General & Plastic Surgery
90d