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 Medical Laser, Inc. with 8 510(k) clearances. The most recent is a 510(k) clearance dated Nov 1, 1991: LASER ENDOSCOPE DISC DECOMPRESSION KITS.
| Nov 1, 1991 | LASER ENDOSCOPE DISC DECOMPRESSION KITSK913136 · LRO | 510(k) clearances |
| Oct 10, 1991 | MEDILASE SEMI-RIGID INSTROD SHEATH SERIES AE1000K912265 · FED | 510(k) clearances |
| Sep 27, 1991 | SERIES 5000 ENDOSCOPE CONSOLE MODELS 5100 AND 5200K912447 · FET | 510(k) clearances |
| Aug 12, 1991 | MODIFIED SERIES 2100 ENDOSCOPESK912089 · ODF | 510(k) clearances |
| Aug 7, 1990 | MEDILASE SERIES 2200 ENDOSCOPEK901464 · GCM | 510(k) clearances |
| Jun 22, 1990 | MEDILASE SERIES 2100 ENDOSCOPEK900894 · GCQ | 510(k) clearances |
| May 15, 1990 | MEDILASE 5010 ENDOSCOPE CONSOLEK900380 · FET | 510(k) clearances |
| Dec 14, 1989 | MEDILASE SYSTEM 2010L LASER LITHOTRIPTORK895837 · 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
