Medical Device Manufacturer · US , Derwood , MD

Tecnoideal America - FDA 510(k) Cleared Devices

1 submissions · 1 cleared · Since 2024
1
Total
1
Cleared
0
Denied

Tecnoideal America has 1 FDA 510(k) cleared medical devices. Based in Derwood, US.

Latest FDA clearance: Feb 2024. Active since 2024. Primary specialty: Gastroenterology & Urology.

Browse the FDA 510(k) cleared devices submitted by Tecnoideal America Filter by specialty or product code using the sidebar.

FDA 510(k) cleared devices by Tecnoideal America

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