Matech, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Matech, Inc. - FDA 510(k) Cleared Devices
6
Total
6
Cleared
0
Denied
Matech, Inc. has 6 FDA 510(k) cleared medical devices. Based in Sylmar, US.
Historical record: 6 cleared submissions from 1994 to 2001. Primary specialty: Dental.
Browse the FDA 510(k) cleared devices submitted by Matech, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Matech, Inc.
6 devices
Cleared
Feb 15, 2001
DURABOND NON-PRECIOUS CERAMIC ALLOY
Dental
38d
Cleared
Dec 13, 1999
CERADIUM V NON-PRECIOUS CERAMIC ALLOY
Dental
53d
Cleared
Nov 19, 1999
HI BOND NON-PRECIOUS CERAMIC ALLOY
Dental
85d
Cleared
Sep 22, 1999
CERADIUM NON-PRECIOUS CERAMIC ALLOY
Dental
42d
Cleared
Feb 12, 1998
KROMATICA COLOR CHANGING ALGINATE
Dental
43d
Cleared
Jan 21, 1994
REPLICA
Dental
434d