Orthomatrix, Inc. is one of 24929 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Orthomatrix, Inc. - FDA 510(k) Cleared Devices
Recent clearances: CANNULATED PLUS SCREW SYSTEM, ORTHOMATRIX, INC. CERCLAGE SYSTEM, MAGELLAN TIBIAL INTRAMEDULLARY NAIL
8
Total
8
Cleared
0
Denied
Orthomatrix, Inc. has 8 FDA 510(k) cleared medical devices. Based in Walker, US.
Historical record: 8 cleared submissions from 1984 to 2001. Primary specialty: Orthopedic.
Browse the FDA 510(k) cleared devices submitted by Orthomatrix, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Orthomatrix, Inc.
8 devices
Cleared
Aug 01, 2001
CANNULATED PLUS SCREW SYSTEM
Orthopedic
142d
Cleared
Dec 13, 2000
ORTHOMATRIX, INC. CERCLAGE SYSTEM
Orthopedic
238d
Cleared
Mar 10, 2000
MAGELLAN TIBIAL INTRAMEDULLARY NAIL
Orthopedic
199d
Cleared
Mar 10, 2000
MAGELLAN HUMERAL INTRAMEDULLARY NAIL
Orthopedic
199d
Cleared
Oct 21, 1985
HA-1000 & HA-500 HYDROXYLAPATITE TOOTH ROOT SUBSTI
Dental
115d
Cleared
Sep 23, 1985
HA-2000 HYDROXYLAPATITE
Dental
87d
Cleared
May 21, 1985
HA-1000 & HA-500 HYDROXYLAPATITE-MODIFICATION
Chemistry
46d
Cleared
Aug 09, 1984
RIDGEMATRIX 20/40 MESH, PERIOMATRIX
Dental
71d