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 15, 2026, FDA's public records list Apoza Enterprise with 5 510(k) clearances. The most recent is a 510(k) clearance dated Mar 2, 2007: APOZA LED CURING LIGHT, MODEL E-MORLIT, D-2000, TOP 3W, TOP 5W.
| Mar 2, 2007 | APOZA LED CURING LIGHT, MODEL E-MORLIT, D-2000, TOP 3W, TOP 5WK070373 · EBZ | 510(k) clearances |
| Jun 18, 2004 | LED TURBO-PENK041303 · EBZ | 510(k) clearances |
| Apr 30, 2004 | APOZA ULTRASONIC SCALER AND EDODONTICS UNIT, SELECTOR U2K033198 · ELC | 510(k) clearances |
| Mar 25, 2004 | LED TURBOK040618 · EBZ | 510(k) clearances |
| Dec 2, 2003 | LA500 BLUE LIGHTK033201 · EBZ | 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
