Theo Manufacturing BV is one of 18408 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Theo Manufacturing BV - FDA 510(k) Cleared Devices
Recent clearances: L-Mesitran Dressing Family II- Soft and Tulle, L-MESITRAN HYDRO, L-MESITRAN BORDER, L-MESITRAN NET, L-MESITRAN ACTIVE
2
Total
2
Cleared
0
Denied
Theo Manufacturing BV has 2 FDA 510(k) cleared medical devices. Based in Bailey, US.
Historical record: 2 cleared submissions from 2007 to 2015. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Theo Manufacturing BV Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Theo Manufacturing BV
2 devices