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 Mnlase, Inc. with 22 510(k) clearances. The most recent is a 510(k) clearance dated Nov 9, 1994: MODEL 230-SAS LASER DELIVERY PROBE.
| Nov 9, 1994 | MODEL 230-SAS LASER DELIVERY PROBEK944630 · GEX | 510(k) clearances |
| Nov 3, 1994 | MODEL 220-SC CURVED ENDOPHOTOCOAGULATOR LASERK944627 · GEX | 510(k) clearances |
| Nov 3, 1994 | CURVED ENDOPHOTOCOAGULATOR LASER PROBEK944470 · GEX | 510(k) clearances |
| Nov 3, 1994 | MODEL 220-SS LASER DELIVERY PROBEK944628 · GEX | 510(k) clearances |
| Nov 3, 1994 | MODEL 210-AS ASPIRATING ENDOPHOTOCOAGULATOR LASERK944626 · GEX | 510(k) clearances |
| Nov 3, 1994 | MODEL 230-SAC LASER DELIVERY PROBEK944629 · GEX | 510(k) clearances |
| Nov 3, 1994 | MODEL 210-AC ASPIRATING ENDOPHOTOCOAGULATOR LASERK944625 · GEX | 510(k) clearances |
| Nov 3, 1994 | STRAIGHT ENDOPHOTOCOAGULATOR LASER PROBEK944471 · 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
