Trumpf Medizin Systeme GmbH + Co. KG is one of 24684 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Trumpf Medizin Systeme GmbH + Co. KG - FDA 510(k) Cleared Devices
Recent clearances: ILED 3 MOBILE (I300M), TRULIGHT 5500 MOBILE (T500M), TRULIGHT 5300 MOBILE (T300M)
1
Total
1
Cleared
0
Denied
Trumpf Medizin Systeme GmbH + Co. KG has 1 FDA 510(k) cleared medical devices. Based in Charleston, US.
Historical record: 1 cleared submissions from 2009 to 2009. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Trumpf Medizin Systeme GmbH + Co. KG Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Trumpf Medizin Systeme GmbH + Co. KG
1 devices