# Ahp Eos Buyer, Inc.

- Location (FDA's records): Parsippany
- FDA decisions: 4 (1979–1987): 4 original PMA approvals
- Product codes: LOE (2), LOF (2)
- Predicates its devices cite: 0 (0 its own); citations of its devices by later devices: 0 (0 its own)
- Recalls linked to its devices: 8 (4 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Recent decisions
- P850035: SpF® Implantable Spinal Fusion Stimulator (Apr 30, 1987)
- P850022: Biomet® OrthoPak® Non-invasive Bone Growth Stimulator System; Biomet® SpinalPak® Non-invasive Spine Fusion Stimulator Sy (Feb 18, 1986)
- P790005: OsteoGenTM Implantable Bone Growth Stimulators (Jan 25, 1980)
- P790002: Biomet (R) EBI BONE Healing System (Nov 6, 1979)

Source page: https://510kreport.com/company/ahp-eos-buyer