Medical Device Manufacturer · US , Utica , NY

Trindium Corp. of America - FDA 510(k) Cleared Devices

1 submissions · 1 cleared · Since 1985
1
Total
1
Cleared
0
Denied

Trindium Corp. of America has 1 FDA 510(k) cleared medical devices. Based in Utica, US.

Historical record: 1 cleared submissions from 1985 to 1985. Primary specialty: Dental.

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

FDA 510(k) Regulatory Record - Trindium Corp. of America

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