Medical device makerLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field. in IsraelLabelled 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 13, 2026, FDA's public records list Curelight with 6 510(k) clearances. The most recent is a 510(k) clearance dated Oct 6, 2004: MULTICLEAR XL MULTIWAVELENGTH TARGETED PHOTOTHERAPY SYSTEM.
| Date | Record | Source |
|---|---|---|
| Oct 6, 2004 | MULTICLEAR XL MULTIWAVELENGTH TARGETED PHOTOTHERAPY SYSTEMK041994 · GEX | 510(k) clearances |
| Jun 30, 2004 | CLEAR100 PHOTOTHERAPY SYSTEM, MODEL FGCM0002K041569 · GEX | 510(k) clearances |
| Apr 15, 2004 | RECLEAR PHOTOTHERAPY SYSTEM, MODEL FGCM0012K033183 · GEX | 510(k) clearances |
| Nov 28, 2003 | MULTICLEAR MULTIWAVELENGTH TARGETED PHOTOTHERAPY SYSTEMK032383 · GEX | 510(k) clearances |
| Feb 12, 2003 | ICLEAR PHOTOTHERAPY SYSTEM, MODEL FGCM0002K030338 · GEX | 510(k) clearances |
| Aug 16, 2002 | CLEARLIGHT PHOTOTHERAPHY SYSTEM, MODEL CL 420K013623 · 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
