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.
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