Medental Intl. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Medental Intl. - FDA 510(k) Cleared Devices
7
Total
7
Cleared
0
Denied
Medental Intl. has 7 FDA 510(k) cleared medical devices. Based in Evergreen, US.
Historical record: 7 cleared submissions from 1997 to 1999. Primary specialty: Dental.
Browse the FDA 510(k) cleared devices submitted by Medental Intl. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Medental Intl.
7 devices
Cleared
Apr 02, 1999
MULTI-CURE COMPOSITE CEMENT
Dental
60d
Cleared
Oct 22, 1998
ZINC PHOSPHATE CEMENT
Dental
55d
Cleared
Sep 30, 1998
MEDENTAL GLASS IONOMER CEMENT TYPE I AND MIRAGE GLASS IONOMER CEMENT TYPE 1
Dental
54d
Cleared
Sep 14, 1998
CHEMICAL CURE COMPOSITE WITH ENAMEL BOND
Dental
84d
Cleared
Jul 31, 1998
POLYCARBOXYLATE CEMENT
Dental
136d
Cleared
Dec 16, 1997
CAVITY VARNISH (INTERMEDIARY VARNISH AND DENTINAL TUBULI SEAL)
Dental
62d
Cleared
Nov 25, 1997
MEDENTAL CHEMICAL CURING SEALANT PIT & FISSURE TINTED
Dental
68d