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 American Laser Corp. with 5 510(k) clearances. The most recent is a 510(k) clearance dated Apr 5, 2001: NUVOLASE 532 MEDICAL LASER SYSTEM.
| Apr 5, 2001 | NUVOLASE 532 MEDICAL LASER SYSTEMK010046 · GEX | 510(k) clearances |
| May 17, 1999 | BQ/BM INTEGRATED LASER DELIVERY SYSTEMK990665 · HQF | 510(k) clearances |
| Mar 22, 1999 | NUVOLASE 532 LASER SYSTEMK990725 · GEX | 510(k) clearances |
| Jan 7, 1983 | LASER PHOTOCOAGULATORK827819 · | 510(k) clearances |
| Jan 22, 1982 | LASER PHOTOCOAGULATOR ARGON MED. LASERK813429 · HPJ | 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
