Energist, Ltd. is one of 176 FDA 510(k) medical device manufacturers from United Kingdom in the dataset, ranked by real submission volume.
Energist, Ltd. - FDA 510(k) Cleared Devices
3
Total
3
Cleared
0
Denied
Energist, Ltd. has 3 FDA 510(k) cleared medical devices. Based in Swansea, GB.
Historical record: 3 cleared submissions from 2006 to 2013. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Energist, Ltd. Filter by specialty or product code using the sidebar.
Energist, Ltd. — FDA 510(k) Products and Clearance History
3 devices
Cleared
Dec 12, 2013
NEOGEN PSR SYSTEM
General & Plastic Surgery
100d
Cleared
Feb 06, 2009
ENERGIST ULTRAPLUS VARIABLE PULSED LIGHT (VPL) SYSTEM
General & Plastic Surgery
134d
Cleared
Mar 16, 2006
ENERGIST ULTRA VPL INTENSE PULSE LIGHT SYSTEM
General & Plastic Surgery
48d