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 Endotherapeutics with 7 510(k) clearances. The most recent is a 510(k) clearance dated Jun 9, 1987: UROSCAN.
| Jun 9, 1987 | UROSCANK870855 · FAP | 510(k) clearances |
| Mar 17, 1986 | ENDOPORT 5MM SINGLE-USE TROCAR AND SLEEVEK860192 · HET | 510(k) clearances |
| Feb 12, 1986 | MOD. ENDONEEDLE SINGLE-USE PNEUMOPERITONEUM NEEDLEK860102 · FHP | 510(k) clearances |
| Feb 12, 1986 | MOD. ENDOPORT SINGLE-USE TROCAR AND SLEEVEK860103 · GCP | 510(k) clearances |
| Aug 13, 1985 | ENDOPORT 5MMK852031 · HET | 510(k) clearances |
| Jan 9, 1985 | ENDONEEDLEK844619 · FHO | 510(k) clearances |
| Jun 28, 1984 | ENDOPORT EROCARK841716 · FBQ | 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
