Medical Device Manufacturer · US , Walker , MI

Unisplint Corp. - FDA 510(k) Cleared Devices

2 submissions · 2 cleared · Since 1982

Total

Cleared

Denied

Unisplint Corp. has 2 FDA 510(k) cleared medical devices. Based in Walker, US.

Historical record: 2 cleared submissions from 1982 to 1983. Primary specialty: Dental.

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

Unisplint Corp. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.

FDA 510(k) Regulatory Record - Unisplint Corp.

2 devices

1-2 of 2