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 biolitec AG and its 1 subsidiaries with 37 510(k) clearances. The most recent is a 510(k) clearance dated Apr 24, 2012: EVOLVE HPD 980/ 1470NM MULTIWAVELENGTH DIODE LASER (EVOLVE DUAL).
| Date | Record | Source |
|---|---|---|
| Apr 24, 2012 | EVOLVE HPD 980/ 1470NM MULTIWAVELENGTH DIODE LASER (EVOLVE DUAL)K120231 · GEX | 510(k) clearances |
| Mar 13, 2012 | MEGABEAM REUSABLE FIBER OPTIC DELIVERY SYSTEMK113688 · GEX | 510(k) clearances |
| Jan 24, 2012 | MEGABEAM ENDO-ENT PROBEK113858 · GEX | 510(k) clearances |
| Jan 20, 2012 | MEGABEAM FIBER OPTIC DELIVERY SYSTEM WITH ADDITIONAL TIPS & HANDPIECEK113709 · GEX | 510(k) clearances |
| Jan 19, 2012 | MEGABEAM ENDOCULAR PROBE AND ASPIRATING ENDOCULAR PROBEK113792 · GEX | 510(k) clearances |
| Jan 13, 2012 | EVOLVE(R) HPD 980/1470NM MULTIWAVELENGTH DIODE LASERK112013 · GEX | 510(k) clearances |
| Dec 16, 2011 | TWISTER SIDE FIRE OPTICAL FIBER DELIVERY SYSTEMK112987 · GEX | 510(k) clearances |
| Nov 3, 2011 | ENDOVASCULAR LASER VEIN SYSTEM KITK112299 · 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
