Medical Device Manufacturer · US , Raleigh , NC

Trinity Laboratories, Inc. - FDA 510(k) Cleared Devices

44 submissions · 28 cleared · Since 1990
44
Total
28
Cleared
0
Denied

Trinity Laboratories, Inc. has 28 FDA 510(k) cleared medical devices. Based in Raleigh, US.

Historical record: 28 cleared submissions from 1990 to 1998.

Browse the FDA 510(k) cleared devices submitted by Trinity Laboratories, Inc. Filter by specialty or product code using the sidebar.

FDA 510(k) Regulatory Record - Trinity Laboratories, Inc.
44 devices
1-12 of 44

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