Tutogen Medical U.S., Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Tutogen Medical U.S., Inc. - FDA 510(k) Cleared Devices
2
Total
2
Cleared
0
Denied
Tutogen Medical U.S., Inc. has 2 FDA 510(k) cleared medical devices. Based in Alachua, US.
Historical record: 2 cleared submissions from 2000 to 2008. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Tutogen Medical U.S., Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Tutogen Medical U.S., Inc.
2 devices