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 American Surgical Laser, Inc. with 5 510(k) clearances. The most recent is a 510(k) clearance dated Feb 4, 1985: MINUTEMAN CO2 MICROSURGICAL LASER GYN.
| Feb 4, 1985 | MINUTEMAN CO2 MICROSURGICAL LASER GYNK843515 · HHR | 510(k) clearances |
| Dec 7, 1984 | MINUTEMAN CO2 MICROSURG LASER DERMATOL-K843517 · GEY | 510(k) clearances |
| Dec 7, 1984 | MINUTEMAN C02 MICROSURG LASER PODIATRYK843518 · GEY | 510(k) clearances |
| Dec 7, 1984 | MINUTEMAN CO2 MICROSURG LASER GEN SURGK843519 · GEY | 510(k) clearances |
| Dec 4, 1984 | MINUTEMAN CO2 MICROSURGICAL LASER OTOK843514 · EWG | 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
