Medical device makerLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field.. FDA records under its name, each linked to the record.
As of Nov 14, 2026, FDA's public records list Unicep with 9 510(k) clearances. The most recent is a 510(k) clearance dated May 27, 1993: MICODOSE CHLORHEXIPREP.
| May 27, 1993 | MICODOSE CHLORHEXIPREPK925163 · ECM | 510(k) clearances |
| Mar 16, 1993 | MICRODOSE PORCELAIN ETCHANTK924821 · ELL | 510(k) clearances |
| Mar 16, 1993 | MICRODOSE DENTIN CONDITIONERK925162 · EBF | 510(k) clearances |
| Mar 16, 1993 | MICRODOSE PIT AND FISSURE SEALANT-CLEAR OR WHITEK924824 · EBC | 510(k) clearances |
| Mar 16, 1993 | MICRODOSE SILANEK924823 · ELL | 510(k) clearances |
| Mar 5, 1993 | MICRODOSE TOTAL ETCHANTK924826 · EBF | 510(k) clearances |
| Mar 5, 1993 | MICRODOSE POTASSIUM OXYLATEK924827 · LBH | 510(k) clearances |
| Mar 5, 1993 | MICRODOSE ENAMEL ETCHANTK924822 · EBF | 510(k) clearances |
Spellings are joined only when they reduce to the same name, or a reviewed source names the same company. Sharing an FDA establishment number (FEI) is not enough: contract sites make products for many firms. Facts marked AI were labelled by a language model from the firm's FDA names; everything else comes from FDA or Wikidata. How this page is built
