# Xanmed Corp.

- Location (FDA's records): Washington, DC
- FDA decisions: 9 (1984–1987): 9 510(k) clearances
- Product codes: DYB (3), LXH (1), HBA (1), KNA (1), HMP (1)
- Predicates its devices cite: 0 (0 its own); citations of its devices by later devices: 0 (0 its own)
- Recalls linked to its devices: 0 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Recent decisions
- K864623: Obstetrical/Gynecological Custom Surgical Kit (Jan 14, 1987)
- K844595: Orthopedic Custom Surgical Kit (Aug 21, 1985)
- K844596: Emergency Room & Minor Office Procedure Custom Kit (Aug 1, 1985)
- K844593: Cardiovascular Custom Surgical Kit (Jun 21, 1985)
- K844594: Neuro Custom Surgical Kit (Jun 13, 1985)
- K851906: Surgical Eye Pack (May 21, 1985)
- K844597: Miscellaneous General Surgical Custom Kit (Apr 8, 1985)
- K843641: Catheter Introducer System (Oct 23, 1984)

Source page: https://510kreport.com/company/xanmed