Theradome, Inc. - FDA 510(k) Cleared Devices
5
Total
5
Cleared
0
Denied
FDA 510(k) Regulatory Record - Theradome, Inc. General & Plastic Surgery ✕
5 devices
Cleared
May 18, 2018
Theradome LH40
General & Plastic Surgery
87d
Cleared
Jan 09, 2018
Theradome LH80 PRO
General & Plastic Surgery
209d
Cleared
May 12, 2016
Laser Helmet LH40-EVO
General & Plastic Surgery
29d
Cleared
Jun 14, 2013
LASER HELMET
General & Plastic Surgery
262d
Cleared
Mar 02, 2012
LASER HELMET
General & Plastic Surgery
135d