Depilase Group , Ltd. is one of 195 FDA 510(k) medical device manufacturers from United Kingdom in the dataset, ranked by real submission volume.
Depilase Group , Ltd. - FDA 510(k) Cleared Devices
7
Total
7
Cleared
0
Denied
Depilase Group , Ltd. has 7 FDA 510(k) cleared medical devices. Based in London Sw1 Y 4rb, GB.
Historical record: 7 cleared submissions from 2000 to 2003. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Depilase Group , Ltd. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Depilase Group , Ltd.
7 devices
Cleared
May 20, 2003
DEPILASE TRIO LASE LASER SYSTEM
General & Plastic Surgery
90d
Cleared
May 14, 2003
DEPILASE TWIN YAG LASER SYSTEM
General & Plastic Surgery
84d
Cleared
May 09, 2003
DEPILASE YAG LASE PLUS LASER SYSTEM
General & Plastic Surgery
79d
Cleared
Apr 12, 2002
DEPILASE TWIN YAG LASER SYSTEM
General & Plastic Surgery
39d
Cleared
Feb 27, 2002
DEPILASE YAG LASE PLUS LASER SYSTEM
General & Plastic Surgery
15d
Cleared
Feb 22, 2002
DEPILASE TWIN LASE LASER SYSTEM
General & Plastic Surgery
15d
Cleared
Oct 23, 2000
DEPILASE YAGLASE ND:YAG LASER SYSTEM AND ACCESSORIES
General & Plastic Surgery
116d