Tecnoideal America - FDA 510(k) Cleared Devices
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.
510(k) submissions have been managed by Amarex Clinical Research, LLC as regulatory consultant.
FDA 510(k) Regulatory Record - Tecnoideal America
1 devices