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., part of AlconLabelled 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 15, 2026, FDA's public records list Alcon LenSx with 2 510(k) clearances and 1 device recall. The most recent is a device recall dated Mar 14, 2014: Alcon LenSx Ophthalmic Laser, for use in cataract surgery for the creation of corneal c….
| Mar 14, 2014 | Alcon LenSx Ophthalmic Laser, for use in cataract surgery for the creation of corneal cuts/incisions, anterior capsulotomy and laser phacofClass II · Alcon LenSx received reports of unexpected downward motion of the gantry. | Device recalls |
| Dec 12, 2012 | LENSX LASER SYSTEMK123120 · OOE | 510(k) clearances |
| Sep 6, 2012 | LENSSX LASER SYSTEMK120732 · HQC | 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
