Medical device makerLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field. in GermanyLabelled 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 Asclepion-Meditec with 5 510(k) clearances. The most recent is a 510(k) clearance dated Sep 13, 2002: LASERSYSTEM BEAUTYSTAR 532.
| Sep 13, 2002 | LASERSYSTEM BEAUTYSTAR 532K021975 · GEX | 510(k) clearances |
| Mar 8, 2002 | DERMASTAR ER:YAG LASER SYSTEMK014057 · GEX | 510(k) clearances |
| Feb 26, 2002 | LASER SYSTEM YELLOWSTARK013940 · GEX | 510(k) clearances |
| Dec 27, 2000 | PHACOFRAGMENTATION SYSTEM MEGATRONK002031 · HQC | 510(k) clearances |
| Sep 11, 2000 | C02 LASER MULTIPULSEK002032 · 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
