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 biolitec AGLabelled 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 15, 2026, FDA's public records list biolitec Medical Devices with 9 510(k) clearances. The most recent is a 510(k) clearance dated Apr 24, 2012: EVOLVE HPD 980/ 1470NM MULTIWAVELENGTH DIODE LASER (EVOLVE DUAL).
| 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 |
| 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 |
| Sep 30, 2011 | RADIAL-EMITTING SHAPED FIBER OPTIC DELIVERY SYSTEMK112442 · 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
