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 14, 2026, FDA's public records list Xanmed with 9 510(k) clearances. The most recent is a 510(k) clearance dated Jan 14, 1987: OBSTETRICAL/GYNECOLOGICAL CUSTOM SURGICAL KIT.
| Jan 14, 1987 | OBSTETRICAL/GYNECOLOGICAL CUSTOM SURGICAL KITK864623 · KNA | 510(k) clearances |
| Aug 21, 1985 | ORTHOPEDIC CUSTOM SURGICAL KITK844595 · LXH | 510(k) clearances |
| Aug 1, 1985 | EMERGENCY ROOM & MINOR OFFICE PROCEDURE CUSTOM KITK844596 · | 510(k) clearances |
| Jun 21, 1985 | CARDIOVASCULAR CUSTOM SURGICAL KITK844593 · DYB | 510(k) clearances |
| Jun 13, 1985 | NEURO CUSTOM SURGICAL KITK844594 · HBA | 510(k) clearances |
| May 21, 1985 | SURGICAL EYE PACKK851906 · HMP | 510(k) clearances |
| Apr 8, 1985 | MISCELLANEOUS GENERAL SURGICAL CUSTOM KITK844597 · | 510(k) clearances |
| Oct 23, 1984 | CATHETER INTRODUCER SYSTEMK843641 · DYB | 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
