Medical Device Manufacturer · US , Carlsbad , CA

Lancer Orthodontics, Inc. - FDA 510(k) Cleared Devices

14 submissions · 14 cleared · Since 1990

Total

Cleared

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. is one of 5229 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.

Lancer Orthodontics, Inc. — FDA 510(k) Products and Clearance History

14 devices

1-12 of 14

ORTHODONTIC BONDING ADHESIVE CONTROL

K904090 · DYH

Dental · 235d

Cleared Nov 09, 1990

LANCER ORIGINAL, SIERRA, GENERAL PURPOSE

K904092 · EJF

Dental · 64d

Cleared Nov 07, 1990

BUCCAL TUBE, BUCCAL ATTACHMENT

K904093 · EJF

Dental · 62d

Cleared Nov 05, 1990

TITANAL,STERLING SPRING,DUAL FLEX,MEMOREX,BENDALLO

C.A.T.,SINTERLINE,NATURAL ARCH,MICROTWIN,BIOTORQUE

K904094 · EJF

Dental · 57d

Cleared Aug 06, 1990

INTRIGUE CERAMIC BRACKET

Lancer Orthodontics, Inc. - FDA 510(k) Cleared Devices

Lancer Orthodontics, Inc. — FDA 510(k) Products and Clearance History

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