Biophotas, Inc. - FDA 510(k) Cleared Devices
6
Total
6
Cleared
0
Denied
Biophotas, Inc. has 6 FDA 510(k) cleared medical devices. Based in Laguna Nuguel, US.
Last cleared in 2023. Active since 2013. Primary specialty: Physical Medicine.
Browse the FDA 510(k) cleared devices submitted by Biophotas, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) cleared devices by Biophotas, Inc.
6 devices
Cleared
Nov 21, 2023
Biophotas Celluma CONTOUR
General & Plastic Surgery
61d
Cleared
Jun 29, 2021
Biophotas Celluma RESTORE
General & Plastic Surgery
83d
Cleared
Sep 01, 2017
BIOPHOTAS CELLUMA3
General & Plastic Surgery
119d
Cleared
Mar 02, 2016
BioPhotas Celluma3
Physical Medicine
203d
Cleared
Jan 15, 2014
BIOPHOTAS CELLUMA
Physical Medicine
268d
Cleared
Jan 03, 2013
BIOPHOTAS LIFELIGHT
Physical Medicine
161d