# Phoenix Medical Technology, Inc.

- Location (FDA's records): Andrews, SC
- FDA decisions: 11 (1986–2000): 11 510(k) clearances
- Product codes: LYY (5), LYZ (3), KGX (1), LZA (1), DRX (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
- K000223: Nitrile Patient Examination Gloves, Powder-Free (Apr 14, 2000)
- K945045: Patient Exaination Gloves (Jan 2, 1995)
- K905031: Patient Examination Gloves (Jan 18, 1991)
- K900454: Modified Low Powder Single Use Latex Exam Gloves (Feb 13, 1990)
- K900453: Modified Single Use Latex Examination Gloves (Feb 13, 1990)
- K890917: Phoenix Drapes with Microban (Aug 17, 1989)
- K892976: Single Use Vinyl Exam Gloves - Color Coded (Jun 22, 1989)
- K892975: Low Powder Single Use Latex Exam Gloves (Jun 19, 1989)

Source page: https://510kreport.com/company/phoenix-medical-technology