Medical Device Manufacturer · US , Sandpoint , ID

Unicep - FDA 510(k) Cleared Devices

9 submissions · 9 cleared · Since 1993

Total

Cleared

Denied

Unicep has 9 FDA 510(k) cleared medical devices. Based in Sandpoint, US.

Historical record: 9 cleared submissions from 1993 to 1993. Primary specialty: Dental.

Browse the FDA 510(k) cleared devices submitted by Unicep Filter by specialty or product code using the sidebar.

Unicep is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.

FDA 510(k) Regulatory Record - Unicep

9 devices

1-9 of 9

Cleared May 27, 1993

MICODOSE CHLORHEXIPREP

K925163 · ECM

Dental · 226d

Cleared Mar 16, 1993

MICRODOSE PORCELAIN ETCHANT

MICRODOSE PIT AND FISSURE SEALANT-CLEAR OR WHITE

K924824 · EBC

Dental · 169d

Cleared Mar 16, 1993

MICRODOSE DENTIN CONDITIONER

K925162 · EBF

Dental · 154d

Cleared Mar 05, 1993

MICRODOSE ENAMEL ETCHANT

MICRODOSE TOTAL ETCHANT

K924826 · EBF

Dental · 158d

Cleared Mar 05, 1993

MICRODOSE POTASSIUM OXYLATE

K924827 · LBH

Dental · 158d

Unicep - FDA 510(k) Cleared Devices

FDA 510(k) Regulatory Record - Unicep

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