# Carbofix Orthpedics, Ltd.

- Location (FDA's records): Herzeliya, IL
- FDA decisions: 2 (2021–2023): 2 510(k) clearances
- Product codes: MAX (1), ODP (1)
- Predicates its devices cite: 11 (1 its own); citations of its devices by later devices: 1 (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
- CarboFix Orthopedics, Ltd.: 3 (https://510kreport.com/company/carbofix-orthopedics)
- Medos International SARL: 1 (https://510kreport.com/company/medos-international)
- Orthofix, Inc.: 1 (https://510kreport.com/company/orthofix)
- Icotec AG: 1 (https://510kreport.com/company/icotec)
- Back 2 Basics Direct, LLC: 1 (https://510kreport.com/company/back-2-basics-direct)
- Stryker Corp.: 1 (https://510kreport.com/company/stryker)
- Astura Medical: 1 (https://510kreport.com/company/astura-medical)
- Choicespine, LP: 1 (https://510kreport.com/company/choicespine)

## Its most-cited devices
- K203683: CarboClear Lumbar Cage System (2021), cited by 1

## Recent decisions
- K222874: CarboClear Cervical Cage System, CarboClear Cervical VBR System (Jul 26, 2023)
- K203683: CarboClear Lumbar Cage System (Jan 15, 2021)

Source page: https://510kreport.com/company/carbofix-orthpedics