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.. FDA records under its name, each linked to the record.
As of Nov 13, 2026, FDA's public records list Circon Corp. with 6 510(k) clearances. The most recent is a 510(k) clearance dated Oct 26, 1999: TRANSVAGINAL HYDRO LAPAROSCOPY (THL) SYSTEM.
| Date | Record | Source |
|---|---|---|
| Oct 26, 1999 | TRANSVAGINAL HYDRO LAPAROSCOPY (THL) SYSTEMK992544 · HEX | 510(k) clearances |
| Aug 3, 1999 | CIRCON SURGIFLEX WAVE TSUNAMI SUCTION-IRRIGATION SYSTEMK992126 · GCX | 510(k) clearances |
| Jul 30, 1998 | SNAP-N-PEEL INTRODUCERSK981611 · KNY | 510(k) clearances |
| Jun 12, 1998 | RIGID CULDOSCOPE AND ACCESSORIESK980972 · HEW | 510(k) clearances |
| May 12, 1998 | USA ELITE SYSTEM VAPORTRODE VAPORIZATION ELECTRODE AND VAPORTOME RESECTION ELECTRODEK973820 · FAS | 510(k) clearances |
| Aug 15, 1997 | VAPORTRODE VAPORIZATION ELECTRODE -GROOVED/FLUTED/SPIKED(GVE-B,GVE-F,GVE-S) & VAPORTOMME VAPORIZATION LOOP (GVE-LG)K964594 · KNF | 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
