Livetec GmbH is one of 5098 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Livetec GmbH - FDA 510(k) Cleared Devices
3
Total
3
Cleared
0
Denied
Livetec GmbH has 3 FDA 510(k) cleared medical devices. Based in Littleton, US.
Historical record: 3 cleared submissions from 2013 to 2015. Primary specialty: Physical Medicine.
Browse the FDA 510(k) cleared devices submitted by Livetec GmbH Filter by specialty or product code using the sidebar.
Livetec GmbH — FDA 510(k) Products and Clearance History
3 devices
Cleared
Jan 13, 2015
3B Laser 500, 3B Laser 200, LA-X P 500, LA-X P 200
Physical Medicine
112d
Cleared
Nov 07, 2014
Power Twin21-50/Power Twin21-100
Physical Medicine
87d
Cleared
Oct 10, 2013
3B LASER NEEDLE
Physical Medicine
114d