Unitek Corp.
Unitek Corp. holds FDA 510(k) medical device clearances, first cleared 1980, most recent 1994.
Top product codes for Unitek Corp.
Recent clearances by Unitek Corp.
- K944286 — METAL-LINED TRANSCEND CERAMIC BRACKET
- K933501 — ALASTIK
- K940165 — ALASTIK
- K923999 — ALASTIK NS
- K924645 — TRANSCEND SERIES 6000 DEBONDING INSTRUMENTS
- K924295 — DEBRACKETING INSTRUMENT
- K923432 — GERMAN MINI DYNALOCK
- K911271 — ADHESIVE PRECOATED BRACKETS
- K910288 — NONSTAINING ALASTIKS
- K890529 — ALASTIGARD
- K880392 — ORTHOLUX VISIBLE LIGHT CURING UNIT
- K880393 — TRANSBOND LIGHT CURED ORTHODONTIC ADHESIVE
- K861965 — UNITEK CERAMIC BRACKET SYSTEM
- K851386 — UNITEK DISPOSABLE IMPRESSION SYRINGE
- K843742 — UNITEK CONVERTIBLE CAP REMOVER TOOL
- K832654 — HEATED GUTTA PERCHA DELIVERY SYSTEM
- K832253 — X-704
- K831098 — DOMINION
- K831096 — STROMA II
- K831097 — CONCERTO
- K812239 — UNITEK PALATAL BAR
- K802515 — ROOT CANAL POST
- K800210 — TONGUE HOLDER/SALIVA EJECTOR
Data sourced from openFDA. This site is unofficial and independent of the FDA.