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.. FDA records under its name, each linked to the record.
As of Nov 13, 2026, FDA's public records list Light Age, Inc. with 7 510(k) clearances. The most recent is a 510(k) clearance dated Apr 3, 2012: EPICARE YAG.
| Date | Record | Source |
|---|---|---|
| Apr 3, 2012 | EPICARE YAGK113115 · GEX | 510(k) clearances |
| Sep 15, 2011 | Q-CLEARK110370 · PDZ | 510(k) clearances |
| Nov 3, 2009 | EPICARE-DUO LASER SYSTEMK091625 · GEX | 510(k) clearances |
| Sep 14, 2004 | LIGHT AGE EPICARE ALEXANDRITE LASER, MODELS 501-1H, 501-SP, 501-LP AND 501-LPXK032991 · GEX | 510(k) clearances |
| Feb 25, 2004 | LIGHT AGE Q-CLEAR LASER, MODEL 701-1101K033259 · GEX | 510(k) clearances |
| Jan 7, 1999 | LIGHT AGE EPICARE ALEXANDRITE LASERK983977 · GEX | 510(k) clearances |
| Feb 17, 1998 | ALEX TA2 ERASERK980131 · GEX | 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
