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 13, 2026, FDA's public records list Lenstec with 6 510(k) clearances. The most recent is a 510(k) clearance dated Nov 29, 2016: Lenstec LC Injection system.
| Date | Record | Source |
|---|---|---|
| Nov 29, 2016 | Lenstec LC Injection systemK161776 · MSS | 510(k) clearances |
| Oct 18, 2013 | LENSTEC LC INJECTION SYSTEMK122848 · MSS | 510(k) clearances |
| Oct 27, 2009 | FLUID ISOLATION DEVICEK091915 · HQC | 510(k) clearances |
| May 7, 2007 | LENSTEC LC INJECTION SYSTEMK063802 · MSS | 510(k) clearances |
| Apr 14, 2006 | LENSTEC INTRAOCULAR LENS (IOL) INJECTION SYSTEMK060533 · MSS | 510(k) clearances |
| May 31, 2005 | LENSTEC INTRAOCULAR LENS (IOL) INJECTION SYSTEM FOR TETRAFLEX INTRAOCULAR LENSESK050638 · MSS | 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
