# Beech Medical Products, Inc.

- Location (FDA's records): Newtown, PA
- FDA decisions: 4 (1993–1997): 4 510(k) clearances
- Product codes: FPA (3), FMI (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
- K972469: Selfshield HN Self Sheathing Hypodermic Needle (Aug 27, 1997)
- K946082: Beech Pro Lok Fixed (Mar 13, 1995)
- K933852: Pro-Lok Extension Set (Dec 29, 1993)
- K933749: Beech Versa Lok (Dec 29, 1993)

Source page: https://510kreport.com/company/beech-medical-products