Sterngold/Implamed is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Sterngold/Implamed - FDA 510(k) Cleared Devices
16
Total
16
Cleared
0
Denied
Sterngold/Implamed has 16 FDA 510(k) cleared dental devices. Based in Attleboro, US.
Historical record: 16 cleared submissions from 1992 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 - Sterngold/Implamed
16 devices
Cleared
Jan 08, 1999
STERNOMEGA TEMPORARY CEMENT AUTOMIX NE, MODEL 220282/220281
Dental
35d
Cleared
Jan 08, 1999
STERNVANTAGE VARNISH LC, MODEL 221001
Dental
35d
Cleared
Nov 13, 1998
STERNGOLD IMPLAMED WIDE PLATFORM DENTAL IMPLANTS AND RELATED PROSTHETICS AND...
Dental
17d
Cleared
Oct 22, 1998
STERNOMEGA BONDING AGENT, STERNOMEGA COMPOSITE LC, STERNOMEGA COMPOMER LC
Dental
80d
Cleared
Oct 09, 1998
STERNOMEGA COMPOMER CEMENT
Dental
53d
Cleared
May 11, 1998
STERNGOLD IMPLAMED HEX SCREW IMPLANT TPS COATED STERNGOLD IMPLAMED HEX SCREW...
Dental
13d
Cleared
Jul 24, 1996
STERNGOLD U-CPF METAL ALLOY (1067800)
Dental
37d
Cleared
Jul 24, 1996
QUASAR YELLOW CROWN AND BRIDGE ALLOY (1122015)
Dental
37d
Cleared
Jul 24, 1996
STERNGOLD BIO-5 (1127210)
Dental
37d
Cleared
Jul 23, 1996
STERNGOLD BIO-4
Dental
36d
Cleared
Jul 18, 1996
PEGASUS DENTAL ALLOY
Dental
31d
Cleared
Jul 18, 1996
STERNGOLD CF
Dental
31d