Medical Device Manufacturer · US , Bailey , CO

Theo Manufacturing BV - FDA 510(k) Cleared Devices

2 submissions · 2 cleared · Since 2007
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
1-2 of 2
Cleared Dec 23, 2015
L-Mesitran Dressing Family II- Soft and Tulle
K150676 · FRO
General & Plastic Surgery · 282d
Cleared Jul 25, 2007
L-MESITRAN HYDRO, L-MESITRAN BORDER, L-MESITRAN NET, L-MESITRAN ACTIVE
K053613 · FRO
General & Plastic Surgery · 575d
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