Lancer Orthodontics, Inc. is one of 5233 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Lancer Orthodontics, Inc. - FDA 510(k) Cleared Devices
14
Total
14
Cleared
0
Denied
Lancer Orthodontics, Inc. has 14 FDA 510(k) cleared dental devices. Based in Carlsbad, US.
Historical record: 14 cleared submissions from 1990 to 2013.
Browse the complete list of FDA 510(k) cleared dental devices from this manufacturer. Filter by specialty or product code using the sidebar.
Lancer Orthodontics, Inc. — FDA 510(k) Products and Clearance History
14 devices
Cleared
Apr 11, 2013
STORM MINI SCREW
Dental
269d
Cleared
Jun 22, 2007
BLUGOO HD
Dental
53d
Cleared
Sep 19, 2005
O.A.S.I. SYSTEM
Dental
98d
Cleared
Aug 11, 1999
PARAGON
Dental
105d
Cleared
Apr 29, 1991
ORTHODONTIC BONDING ADHESIVE CONTROL
Dental
235d
Cleared
Nov 09, 1990
LANCER ORIGINAL, SIERRA, GENERAL PURPOSE
Dental
64d
Cleared
Nov 07, 1990
BUCCAL TUBE, BUCCAL ATTACHMENT
Dental
62d
Cleared
Nov 05, 1990
TITANAL,STERLING SPRING,DUAL FLEX,MEMOREX,BENDALLO
Dental
60d
Cleared
Nov 02, 1990
PERMA MESH
Dental
57d
Cleared
Nov 02, 1990
C.A.T.,SINTERLINE,NATURAL ARCH,MICROTWIN,BIOTORQUE
Dental
57d
Cleared
Aug 06, 1990
INTRIGUE CERAMIC BRACKET
Dental
90d
Cleared
Jul 30, 1990
MUSTANG, C.A.T.
Dental
90d
Cleared
Jul 30, 1990
GUARDIAN SAFE BOW
Dental
90d
Cleared
Apr 10, 1990
SPORTS PACK ELASTICS
Dental
62d