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 Xanar with 12 510(k) clearances. The most recent is a 510(k) clearance dated Oct 3, 1986: XANAR CO2 SURGICAL LASER SYSTEM MODEL XAP-15.
| Date | Record | Source |
|---|---|---|
| Oct 3, 1986 | XANAR CO2 SURGICAL LASER SYSTEM MODEL XAP-15K861688 · GEX | 510(k) clearances |
| Apr 18, 1986 | AMBULASEK852436 · GEX | 510(k) clearances |
| Mar 14, 1986 | MODEL NY-110 FOR UPPER & LOWER (GU) & PULMONARYK860496 · LNK | 510(k) clearances |
| Jan 24, 1986 | MODEL XA-50 - CO2 SURGICAL LASERK853620 · GEX | 510(k) clearances |
| Aug 15, 1985 | CO 2 SURGICAL LASER SYSTEM NA-120K850818 · GEX | 510(k) clearances |
| Aug 15, 1985 | CO 2 SURGICAL LASER SYSTEM MODEL NA-40K850805 · GEX | 510(k) clearances |
| Aug 15, 1985 | CO 2 SURGICAL LASER SYSTEM NA-30K850804 · GEX | 510(k) clearances |
| Feb 27, 1985 | XANAR MODEL XSE-300 SMOKE EVACULATERK844087 · FYD | 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
