Den-Mat Corp. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Den-Mat Corp. - FDA 510(k) Cleared Devices
29
Total
29
Cleared
0
Denied
Den-Mat Corp. has 29 FDA 510(k) cleared dental devices. Based in Mchenry, US.
Historical record: 29 cleared submissions from 1977 to 1999.
Browse the complete list of FDA 510(k) cleared dental devices from this manufacturer. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Den-Mat Corp.
29 devices
Cleared
Feb 09, 1999
1ST IMPRESSION
Dental
158d
Cleared
Aug 03, 1990
DEN-MAT CERINATE PORCELAIN
Dental
311d
Cleared
Feb 22, 1990
DEN-MAT LAMI-QUICK
Dental
183d
Cleared
Jul 15, 1988
LIGHT-CURED ZIONOMER CEMENT
Dental
67d
Cleared
Mar 18, 1988
DEN-MAT PORETCH (PORCELAIN ETCHANT)
Dental
78d
Cleared
Aug 24, 1987
DEN-MAT TENURE
Dental
61d
Cleared
Feb 19, 1987
DEN-MAT SECURE ANTI-ROTATIONAL POST-CORE SYSTEM
Dental
38d
Cleared
Jan 07, 1987
REMBRANDT PORCELAIN TINTING KIT
Dental
64d
Cleared
Jul 22, 1986
DEN-MAT DENTIN LINK
Dental
25d
Cleared
Mar 25, 1986
DEN-MAT GOLD LINK (FORMERLY DEN-MAT METAL OPAQUER)
Dental
21d
Cleared
Dec 18, 1985
DEN-MAT PAINT-ON RUBBER DAM
Dental
181d
Cleared
Jun 20, 1985
ZIONOMER CEMENT
Dental
31d