# Inter-Os Technologies

- Location (FDA's records): Lone Tree, CO
- FDA decisions: 2 (2000–2003): 2 510(k) clearances
- Names in FDA's records: Inter-Os Technologies (1); Inter-Os Technologies, LLC (1)
- Product codes: KTT (1), MQN (1)
- Predicates its devices cite: 8 (1 its own); citations of its devices by later devices: 4 (1 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
- Ebi, L.P.: 3 (https://510kreport.com/company/ebi)
- Synthes (Usa): 2 (https://510kreport.com/company/synthes-usa)
- Electro-Biology, Inc.: 1 (https://510kreport.com/company/electro-biology)
- Orthodyne, Inc.: 1 (https://510kreport.com/company/orthodyne)

## Firms that cite its devices most
- Orthonetx, Inc.: 2 (https://510kreport.com/company/orthonetx)
- Nuvasive Specialized Orthopedics, Inc.: 1 (https://510kreport.com/company/nuvasive-specialized-orthopedics)

## Its most-cited devices
- K031875: Inter-OS Limb Lengthener (2003), cited by 2
- K993869: Inter-OS Bone Generator (2000), cited by 2

## Recent decisions
- K031875: Inter-OS Limb Lengthener (Oct 22, 2003)
- K993869: Inter-OS Bone Generator (Jan 19, 2000)

Source page: https://510kreport.com/company/inter-os-technologies