Medical device makerLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field. in United StatesLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field., part of 3MLabelled 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 13, 2026, FDA's public records list Unitek Corp. with 23 510(k) clearances. The most recent is a 510(k) clearance dated Nov 29, 1994: METAL-LINED TRANSCEND CERAMIC BRACKET.
| Nov 29, 1994 | METAL-LINED TRANSCEND CERAMIC BRACKETK944286 · DYW | 510(k) clearances |
| Apr 28, 1994 | ALASTIKK933501 · EJF | 510(k) clearances |
| Mar 7, 1994 | ALASTIKK940165 · ECI | 510(k) clearances |
| Jun 24, 1993 | ALASTIK NSK923999 · ECI | 510(k) clearances |
| Nov 25, 1992 | TRANSCEND SERIES 6000 DEBONDING INSTRUMENTSK924645 · JEX | 510(k) clearances |
| Nov 23, 1992 | DEBRACKETING INSTRUMENTK924295 · JEX | 510(k) clearances |
| Oct 30, 1992 | GERMAN MINI DYNALOCKK923432 · EJF | 510(k) clearances |
| May 29, 1991 | ADHESIVE PRECOATED BRACKETSK911271 · DYH | 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
