# Barriermed, Inc.

- Location (FDA's records): Lake Mary, FL
- FDA decisions: 3 (1989–2006): 3 510(k) clearances
- Product codes: LZA (1), LYY (1), KGO (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
- K060733: Synthalon PI Powder-Free Synthetic Polyisoprene/Polychloroprene Examination Gloves MDL 1362-10 to 1362-44 (Apr 24, 2006)
- K011446: Barrierplus Powder-Free Synthetic Polyisoprene Surgical Gloves (Jun 14, 2001)
- K890974: Patient Examination Glove (Jul 14, 1989)

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