Medical device makerLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field.. FDA records under 2 spellings of its name, each linked to the record.
As of Nov 13, 2026, FDA's public records list Lightmed Corp. with 10 510(k) clearances. The most recent is a 510(k) clearance dated Jun 15, 2016: LightLas Multi-Wavelength Medical Laser System.
| Date | Record | Source |
|---|---|---|
| Jun 15, 2016 | LightLas Multi-Wavelength Medical Laser SystemK152688 · HQF | 510(k) clearances |
| Feb 27, 2015 | LIGHTMED TRUSCAN 577K142172 · HQF | 510(k) clearances |
| Sep 26, 2013 | LIGHTLAS FAMILY OF MULTI-WAVELENGTH MEDICAL LASER SYSTEMK124043 · HQF | 510(k) clearances |
| Nov 3, 2011 | LIGHTLAS MULTI-WAVELENGTH MEDICAL LASER SYSTEMK103547 · HQF | 510(k) clearances |
| Sep 28, 2009 | LIGHTLAS 577 MEDICAL OPTICAL PUMPED SEMICONDUCTOR LASERK091981 · HQF | 510(k) clearances |
| Sep 18, 2009 | LIGHTLAS MODEL 532K091534 · HQF | 510(k) clearances |
| Aug 13, 2009 | LIGHTLAS SELECTORK090774 · HQF | 510(k) clearances |
| Sep 20, 2007 | LIGHTLAS 561 OPTHALMIC PHOTOCOAGULATORK063297 · HQF | 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
