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 Litecure, LLC with 7 510(k) clearances. The most recent is a 510(k) clearance dated Feb 22, 2018: LightForce LTS Model 1000, 1500, 2500, and 4000.
Drug approvals, 510(k) clearances, recalls and letters, 2017 to 2026 to date
A hatched bar is a year that is not over, so its count covers only part of the year.
| Feb 22, 2018 | LightForce LTS Model 1000, 1500, 2500, and 4000K173067 · GEX | 510(k) clearances |
| Mar 29, 2013 | LITECURE THERAPY SYSTEM MODEL LTS-1500K123014 · PDZ | 510(k) clearances |
| Dec 3, 2012 | BWF-5 MEDICAL LASER SERIESK123031 · GEX | 510(k) clearances |
| Jun 12, 2012 | LITECURE THERAPY COMPACTK121487 · ILY | 510(k) clearances |
| Jan 25, 2011 | LITECURE THERAPY SYSTEMK103511 · ILY | 510(k) clearances |
| May 12, 2010 | BWF-5 MEDICAL LASER SERIESK093087 · GEX | 510(k) clearances |
| Feb 28, 2007 | LC THERAPY, MODEL LCT-1000K070400 · ILY | 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
