Medical Device Manufacturer · US , Mchenry , IL

Unitek Corp. - FDA 510(k) Cleared Devices

23 submissions · 23 cleared · Since 1980

Recent clearances: METAL-LINED TRANSCEND CERAMIC BRACKET, ALASTIK, ALASTIK

Total

Cleared

Denied

Unitek Corp. has 23 FDA 510(k) cleared dental devices. Based in Mchenry, US.

Historical record: 23 cleared submissions from 1980 to 1994.

Browse the complete list of FDA 510(k) cleared dental devices from this manufacturer. Filter by specialty or product code using the sidebar.

Unitek Corp. is one of 14575 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.

FDA 510(k) Regulatory Record - Unitek Corp.

23 devices

1-12 of 23

Cleared Nov 29, 1994

METAL-LINED TRANSCEND CERAMIC BRACKET

TRANSCEND SERIES 6000 DEBONDING INSTRUMENTS

K924645 · JEX

Dental · 72d

Cleared Nov 23, 1992

DEBRACKETING INSTRUMENT

ADHESIVE PRECOATED BRACKETS

ORTHOLUX VISIBLE LIGHT CURING UNIT

K880392 · EBZ

Dental · 69d

Cleared Mar 31, 1988

TRANSBOND LIGHT CURED ORTHODONTIC ADHESIVE

K880393 · DYH

Dental · 62d

Unitek Corp. - FDA 510(k) Cleared Devices

FDA 510(k) Regulatory Record - Unitek Corp.

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