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 Derma-Lase Co. with 5 510(k) clearances. The most recent is a 510(k) clearance dated Oct 15, 1993: MULTILINE; DLY-1.
| Oct 15, 1993 | MULTILINE; DLY-1K932156 · GEX | 510(k) clearances |
| Aug 19, 1993 | MULTILINE; DLY-1K930793 · GEX | 510(k) clearances |
| Aug 19, 1993 | DERMA-LASE DLA-1 LASERK930975 · GEX | 510(k) clearances |
| Jun 4, 1993 | DLR-1 DERMA-LASE RUBY LASER/DLR-1/DERMA-LASE SYSTK924647 · GEX | 510(k) clearances |
| Jan 22, 1992 | DERMA-LASE RUBY LASER - MODEL DLR-1K913256 · 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
