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 13, 2026, FDA's public records list L.A.S.E.R., Inc. with 14 510(k) clearances. The most recent is a 510(k) clearance dated Dec 22, 1998: CO2 LASER COUPLER.
| Date | Record | Source |
|---|---|---|
| Dec 22, 1998 | CO2 LASER COUPLERK983965 · GEX | 510(k) clearances |
| Mar 31, 1995 | REUSABLE TROCAR WITH SAFETY SLEEVEK950021 · GCJ | 510(k) clearances |
| Mar 25, 1994 | GRASPING FORCEPS, PUNCHES, SCISSORSK940454 · HRX | 510(k) clearances |
| Feb 7, 1994 | TROCAR SLEEVEK931561 · HET | 510(k) clearances |
| Nov 2, 1993 | ENDOSCOPIC INSTRUMENTS AND ACCESSDORIESK933421 · GCJ | 510(k) clearances |
| Oct 8, 1993 | BULK TISSUE REMOVAL SYSTEMK924844 · HET | 510(k) clearances |
| Sep 23, 1993 | DISPOSABLE INSUFFLATION TUBINGK932045 · GCJ | 510(k) clearances |
| Apr 30, 1993 | ENDOSCOPIC RETRACTORK931092 · GCJ | 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
