# Biocore9, LLC

- Location (FDA's records): Whippany, NJ
- FDA decisions: 3 (2020–2022): 3 510(k) clearances
- Product codes: LPH (1), KXA (1), HSD (1)
- Predicates its devices cite: 4 (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

## Firms whose devices it cites most
- Endotec, Inc.: 2 (https://510kreport.com/company/endotec)
- Endomedics, Inc.: 1 (https://510kreport.com/company/endomedics)
- Protek, Inc.: 1 (https://510kreport.com/company/protek)

## Recent decisions
- K212761: Biocore9 Acetabular Cup System (May 17, 2022)
- K201219: Biocore9 Femoral Head Resurfacing Component (Jan 19, 2021)
- K193122: Biocore9 Humeral Resurfacing System (May 15, 2020)

Source page: https://510kreport.com/company/biocore9