Medical Device Manufacturer · US , Washington , DC

U.S. Apatite Corp. - FDA 510(k) Cleared Devices

2 submissions · 2 cleared · Since 1988

Total

Cleared

Denied

U.S. Apatite Corp. has 2 FDA 510(k) cleared medical devices. Based in Washington, US.

Historical record: 2 cleared submissions from 1988 to 1988. Primary specialty: Dental.

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

U.S. Apatite 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 - U.S. Apatite Corp.

2 devices

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