Led Technologies, Inc. - FDA 510(k) Cleared Devices
12
Total
12
Cleared
0
Denied
Led Technologies, Inc. has 12 FDA 510(k) cleared general & plastic surgery devices. Based in Greenwood Village, US.
Last cleared in 2022. Active since 2017.
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 Led Technologies, Inc.
12 devices
Cleared
Dec 21, 2022
reVive Light Therapy® Wrinkle and Acne LED Device
General & Plastic Surgery
33d
Cleared
Jul 27, 2022
reVive Light Therapy LED Cleansing System
General & Plastic Surgery
71d
Cleared
Dec 21, 2021
reVive Light Therapy Essentials
General & Plastic Surgery
265d
Cleared
Dec 15, 2021
reVive Light Therapy Essentials
General & Plastic Surgery
259d
Cleared
Mar 14, 2019
dpl Faceware
General & Plastic Surgery
113d
Cleared
Feb 07, 2019
dpl SpotLite
General & Plastic Surgery
90d
Cleared
Jun 04, 2018
reVive Light Therapy LED Cleansing System
General & Plastic Surgery
104d
Cleared
May 15, 2018
reVive Light Therapy LED Ultrasonic Wrinkle System
General & Plastic Surgery
84d
Cleared
Apr 03, 2018
dpl IIa Panel
General & Plastic Surgery
57d
Cleared
Jan 09, 2018
reVive Perioral
General & Plastic Surgery
126d
Cleared
Aug 07, 2017
dpl SpectraLite
General & Plastic Surgery
88d
Cleared
Aug 03, 2017
dpl II Panel
General & Plastic Surgery
84d