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 Surgilase, Inc. with 19 510(k) clearances. The most recent is a 510(k) clearance dated Oct 15, 1993: SURGILASE/OP 15, 20, 25, 30, 40, 50 CO2 SURG. LASE.
| Oct 15, 1993 | SURGILASE/OP 15, 20, 25, 30, 40, 50 CO2 SURG. LASEK932421 · GEX | 510(k) clearances |
| Apr 15, 1993 | SURGILASE FIBERLASE CO2 LASER WAVEGUIDEK924664 · GEX | 510(k) clearances |
| Feb 21, 1991 | SURGILASE SL 150 SURGICAL LASER SYSTEMK905006 · GEX | 510(k) clearances |
| Dec 7, 1990 | SURGILASE SL 50/60 GOLD SURGICAL LASER SYSTEMK904203 · GEX | 510(k) clearances |
| Jun 29, 1990 | SURGILASE YAG 100 SURGICAL LASER SYSTEMK902211 · GEX | 510(k) clearances |
| May 1, 1990 | SURGILASE YAG 100 IN ORTHOPEDIC SURGERYK900570 · GEX | 510(k) clearances |
| Apr 26, 1990 | SURGILASE CO2 SURGICAL LASER SYSTEMS MODEL SL120K901227 · GEX | 510(k) clearances |
| Apr 26, 1990 | SURGILASE SL50 SURGICAL LASER SYSTEMK901211 · 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
