Medical Device Manufacturer · US , Walker , MI

Orthomatrix, Inc. - FDA 510(k) Cleared Devices

8 submissions · 8 cleared · Since 1984

8

Total

8

Cleared

0

Denied

FDA 510(k) Regulatory Record - Orthomatrix, Inc. Dental ✕

3 devices

1-3 of 3

Cleared Oct 21, 1985

HA-1000 & HA-500 HYDROXYLAPATITE TOOTH ROOT SUBSTI

Cleared Sep 23, 1985

HA-2000 HYDROXYLAPATITE

Cleared Aug 09, 1984

RIDGEMATRIX 20/40 MESH, PERIOMATRIX