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 15, 2026, FDA's public records list Ximed with 9 510(k) clearances. The most recent is a 510(k) clearance dated Jan 4, 2001: ELECTROSURGICAL PROBES AND DEVICES-GELTX.
| Jan 4, 2001 | ELECTROSURGICAL PROBES AND DEVICES-GELTXK002269 · GEI | 510(k) clearances |
| Mar 1, 2000 | PERCUTX-INJECTION/ASPIRATION NEEDLE PROBES/DEVICESK994151 · GAA | 510(k) clearances |
| Dec 11, 1998 | INJECTION NEEDLE PROBE/DEVICE-TUNISK983765 · FBK | 510(k) clearances |
| Dec 11, 1998 | INJECTION/ASPIRATION NEEDLES PROBES/DEVICES-TPI/TPI FLEXK983200 · GAA | 510(k) clearances |
| May 12, 1998 | ISOLATED SALINE ELECTRODES/PROBES/DEVICES-SALINETRODEK981256 · FAS | 510(k) clearances |
| Feb 10, 1998 | ISOLATED ELECTROSURGICAL PROBES AND DEVICES-SALINETRODEK974484 · GEI | 510(k) clearances |
| Jan 7, 1998 | ELECTRODES/PROBES/DEVICESK974637 · FAS | 510(k) clearances |
| Nov 12, 1996 | ELECTROSURGICAL PROBES & DEVICESK962593 · GEI | 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
