# Orthogem Limited

- Location (FDA's records): Nottingham, GB
- FDA decisions: 3 (2007–2015): 3 510(k) clearances
- Names in FDA's records: Orthogem Limited (2); Orthogem, Ltd. (1)
- Product codes: MQV (3)
- Predicates its devices cite: 4 (3 its own); citations of its devices by later devices: 4 (3 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
- Micromedics, Inc.: 1 (https://510kreport.com/company/micromedics)

## Firms that cite its devices most
- Biostone, Ltd.: 1 (https://510kreport.com/company/biostone)

## Its most-cited devices
- K070132: Tripore, Models HA, BP90, BP15 (2007), cited by 3
- K110787: Tripore TDD (HA), Tripore TDD (BP90), Tripore TDD (BP15) (2011), cited by 1

## Recent decisions
- K150064: Synthetic Bone Graft (TriPore HA, TriPore BP90, TriPore BP15) (Sep 4, 2015)
- K110787: Tripore TDD (HA), Tripore TDD (BP90), Tripore TDD (BP15) (Apr 21, 2011)
- K070132: Tripore, Models HA, BP90, BP15 (Jul 13, 2007)

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