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 13, 2026, FDA's public records list Endolap, Inc. with 5 510(k) clearances. The most recent is a 510(k) clearance dated Dec 22, 1997: ENDOLAP RESECTOSCOPE CUTTING LOOP ELECTRODE.
| Date | Record | Source |
|---|---|---|
| Dec 22, 1997 | ENDOLAP RESECTOSCOPE CUTTING LOOP ELECTRODEK974516 · FAS | 510(k) clearances |
| Dec 22, 1997 | ENDOLAP RESECTOSCOPE ROLLER ELECTRODEK974515 · FAS | 510(k) clearances |
| Apr 6, 1995 | TITAN INSUFFLATION NEEDLEK950243 · GCJ | 510(k) clearances |
| Mar 23, 1995 | ENDOLAP INSUFFLATOR TUBING SETK950219 · HIF | 510(k) clearances |
| Mar 25, 1994 | ESYS SYSTEMK933492 · HET | 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
