Livetec GmbH is one of 18945 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Livetec GmbH - FDA 510(k) Cleared Devices
Recent clearances: 3B Laser 500, 3B Laser 200, LA-X P 500, LA-X P 200, Power Twin21-50/Power Twin21-100, 3B LASER NEEDLE
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.
510(k) submissions have been managed by Regulatory Insight, Inc. as regulatory consultant.
FDA 510(k) Regulatory Record - Livetec GmbH
3 devices