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 Minnesota Laser Corp. with 12 510(k) clearances. The most recent is a 510(k) clearance dated Jul 12, 1988: ND:YAG SURGICAL LASER FOR GASTRO/UROLOGY APPLICA..
| Jul 12, 1988 | ND:YAG SURGICAL LASER FOR GASTRO/UROLOGY APPLICA.K874253 · LNK | 510(k) clearances |
| Jul 12, 1988 | ND:YAG SURGICAL LASER FOR ENDO. GASTRO/URO. APPLI.K874255 · LNK | 510(k) clearances |
| Mar 4, 1988 | ND:YAG SURGICAL LASER FOR PULMONARY APPLICATIONSK874254 · LLO | 510(k) clearances |
| Jun 20, 1986 | PORTALASE 200 CARBON DIOXIDE SURG LASER NEUROLOGICK854468 · GEX | 510(k) clearances |
| Jun 20, 1986 | PORTALASE 300 CARBON DIOXIDE SURG LASER NEUROLOGICK854473 · GEX | 510(k) clearances |
| Feb 13, 1986 | PORTALASE 300 CARBON DIOXIDE SURG LASER EAR/NOSE/TK854471 · EWG | 510(k) clearances |
| Feb 11, 1986 | PORTALASE 300 CARBON DIOXIDE SURG LASER DERMATOLOGK854472 · GEX | 510(k) clearances |
| Feb 11, 1986 | PORTALASE 200 CARBON DIOXIDE SURG LASER DERMATOLOGK854469 · 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
