Thermolase Corp. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Thermolase Corp. - FDA 510(k) Cleared Devices
3
Total
3
Cleared
0
Denied
Thermolase Corp. has 3 FDA 510(k) cleared medical devices. Based in San Diego, US.
Historical record: 3 cleared submissions from 1995 to 1999. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Thermolase Corp. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Thermolase Corp.
3 devices
Cleared
Dec 23, 1999
SOFTLIGHT Q-SWITCHED ND: YAG LASER WITH OPTIONAL BEAM-SHRINKING HANDPIECE...
General & Plastic Surgery
90d
Cleared
May 13, 1998
SOFTLIGHT Q-SWITCHED (ND:YAG) LASER
General & Plastic Surgery
412d
Cleared
Apr 03, 1995
THERMOLASE LT-100 ND:YAG LASER HAIR REMOVAL SYSTEM
General & Plastic Surgery
90d