Medical device makerLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field. in United StatesLabelled 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 Schwartz Electro-Optics with 9 510(k) clearances. The most recent is a 510(k) clearance dated May 22, 1998: SCHWARTZ ELECTRO-OPTICS, INC. CRYSTALASE 755 DP ALEXANDRITE LASER SYSTEM.
| May 22, 1998 | SCHWARTZ ELECTRO-OPTICS, INC. CRYSTALASE 755 DP ALEXANDRITE LASER SYSTEMK980710 · GEX | 510(k) clearances |
| Mar 19, 1998 | SCHWARTZ ELECTRO-OPTICS, INC. CLR 2940 ERBIUM CRYSTALASEK980313 · GEX | 510(k) clearances |
| Feb 10, 1998 | SCHWARTZ ELECTRO-OPTICS, INC. CRYSTALASE 755 LASER SYSTEMK973867 · GEX | 510(k) clearances |
| Jan 12, 1998 | SCHWARTZ ELECTRO-OPTICS, INC. CLR 2940 ERBIUM CRYSTALASEK974039 · GEX | 510(k) clearances |
| Dec 19, 1997 | SCHWARTZ ELECTRO-OPTICS, INC. CRYSTALASE 1064/532 LASER SYSTEMK973603 · GEX | 510(k) clearances |
| Jul 9, 1997 | SCHWARTZ ELECTRO-OPTICS, INC. CLR 2940/ERBIUM CRYSTALASE (FORMERLY TRILASE 2940 ERBIUM LASERK971404 · GEX | 510(k) clearances |
| Feb 5, 1996 | SCHWARTZ ELECTRO-OPTICES, INC. TRILASE 2100/20 HOLMIUM LASERK953585 · GEX | 510(k) clearances |
| Jan 31, 1996 | TRILASE 2940 ERBIUM LASERK954013 · 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
