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 Medical Systems with 11 510(k) clearances. The most recent is a 510(k) clearance dated Mar 11, 1996: BALLOON ELECTROSURGICAL PROBES AND DEVICES.
| Mar 11, 1996 | BALLOON ELECTROSURGICAL PROBES AND DEVICESK943014 · GEI | 510(k) clearances |
| Mar 24, 1995 | ELECTROPROBE SINGLE USE ELECTROSURGICAL PROBESK946377 · GEI | 510(k) clearances |
| Aug 26, 1994 | HAND-HELD IRRIGATION PUMPK933757 · BTA | 510(k) clearances |
| May 5, 1994 | SURGICAL TROCARSK933458 · GCJ | 510(k) clearances |
| Aug 3, 1993 | UNIVERSAL IRRIGATION & SUCTION TUBING SETK922714 · JOL | 510(k) clearances |
| Sep 23, 1992 | BIPOLAR ELECTROSURGICAL PROBES & INSTRUMENTSK922523 · GEI | 510(k) clearances |
| Sep 20, 1990 | ELECTROPROBE SINGLE-USE SURGICAL PROBEK903812 · GEI | 510(k) clearances |
| Mar 22, 1990 | LASER DELIVERY SYSTEMS, FIBEROPTICS & CONTACT TIPSK900463 · 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
