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 Endo Technic Corp. with 10 510(k) clearances. The most recent is a 510(k) clearance dated May 27, 1999: MILLENNIUM.
| Date | Record | Source |
|---|---|---|
| May 27, 1999 | MILLENNIUMK990908 · MXF | 510(k) clearances |
| Jul 18, 1997 | DERMALASEK971459 · GEX | 510(k) clearances |
| Aug 24, 1994 | LAPAROSCOPIC INST. (SCISSORS,FORCEPS,NEEDLEHOLDER)K925079 · HET | 510(k) clearances |
| Mar 9, 1994 | LAPAROSCOPIC IRRIGATION/ASPIRATION HANDPIECEK930756 · HET | 510(k) clearances |
| Feb 28, 1994 | LAPAROSCOPIC INSTRUMENTSK925114 · HFI | 510(k) clearances |
| Mar 30, 1993 | TROCARK924058 · GCJ | 510(k) clearances |
| Mar 19, 1992 | 1-125 ENDOSEEDK914825 · KXK | 510(k) clearances |
| May 9, 1991 | LASER-35K910200 · 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
