Dent Zar, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Dent Zar, Inc. - FDA 510(k) Cleared Devices
12
Total
12
Cleared
0
Denied
Dent Zar, Inc. has 12 FDA 510(k) cleared dental devices. Based in Los Angeles, US.
Historical record: 12 cleared submissions from 1989 to 1996.
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 - Dent Zar, Inc.
12 devices
Cleared
Jul 03, 1996
SELF CURE BONDING AGENT
Dental
20d
Cleared
Apr 26, 1996
LIGHT SUPER BOND-1 LIGHT CURED ORTHODONTIC ADHESIVE FOR METAL, PLASTIC AND...
Dental
74d
Cleared
Apr 26, 1996
FANTASTIC 1 CONTACT CURE ORTHODONTIC ADHESIVE FOR PLASTIC AND METAL BRACKETS
Dental
74d
Cleared
Apr 26, 1996
ORION-I CORE BUILD-UP MATERIAL CHEMICAL CURE
Dental
74d
Cleared
Apr 26, 1996
ORION-1 VL CROWN BASE AND POST CEMENT VISIBLE LIGHT CURE
Dental
74d
Cleared
Apr 26, 1996
CONCORD MARYLAND BRIDGE CEMENT
Dental
74d
Cleared
Apr 26, 1996
SUPERIOR PHOTOCURING HYBRID COMPOSITE
Dental
74d
Cleared
Apr 26, 1996
LEXUR ENAMEL COATING-PORCELAIN REPAIR-BONDING VENEERS
Dental
74d
Cleared
Apr 26, 1996
ENAMEL CONDITIONER (ENAMEL ETCHING AGENT)
Dental
64d
Cleared
Mar 22, 1996
ACORN ANTERIOR/POSTERIOR COMPOSITE RESTORATIVE
Dental
42d
Cleared
Oct 20, 1989
SKYROCK AND LIGHT SUPERBOND
Dental
88d
Cleared
Jun 09, 1989
ZAROLAN, DUALAN, TITAN AND SUPERON
Dental
81d