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 Endooptiks, Inc. with 5 510(k) clearances. The most recent is a 510(k) clearance dated Mar 3, 2009: ENDO OPTIKS UROLOGICAL CATHETER FOR ENDOSCOPY, MODEL SESSR.
| Mar 3, 2009 | ENDO OPTIKS UROLOGICAL CATHETER FOR ENDOSCOPY, MODEL SESSRK083788 · EYB | 510(k) clearances |
| Nov 22, 2004 | MICROPROBE LASER AND ENDOSCOPY SYSTEM, MODEL E2K042918 · GEX | 510(k) clearances |
| Jan 8, 2001 | MICROPOBE SERIES OF LASERS AND ACCESSORIESK003151 · GEX | 510(k) clearances |
| Mar 6, 1995 | TRANSTYMPANIC ENDOSCOPEK945081 · EOB | 510(k) clearances |
| Sep 28, 1992 | ENDOPROBESK922917 · 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
