# Bespoke Technologies, LLC

- Location (FDA's records): Winston-Salemn, NC
- FDA decisions: 2 (2020–2022): 2 510(k) clearances
- Names in FDA's records: Bespoke Technologies, LLC (1); Bespoke Technologies (1)
- Product codes: OVE (1), ODP (1)
- Predicates its devices cite: 8 (1 its own); citations of its devices by later devices: 3 (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
- Nexxt Spine, LLC: 1 (https://510kreport.com/company/nexxt-spine)
- Additive Implants, Inc.: 1 (https://510kreport.com/company/additive-implants)
- Eminent Spine: 1 (https://510kreport.com/company/eminent-spine)
- Corelink, LLC: 1 (https://510kreport.com/company/corelink)
- Centinel Spine, Inc.: 1 (https://510kreport.com/company/centinel-spine)
- Synthes (Usa): 1 (https://510kreport.com/company/synthes-usa)
- Ht Medical, LLC: 1 (https://510kreport.com/company/ht-medical)

## Firms that cite its devices most
- Keos: 1 (https://510kreport.com/company/keos)
- Southern Medical (Pty), Ltd.: 1 (https://510kreport.com/company/southern-medical)

## Its most-cited devices
- K200458: Tailored-C Cervical Interbody Fusion System (2020), cited by 3

## Recent decisions
- K222903: Tailored-H Cervical Stand Alone System (Nov 18, 2022)
- K200458: Tailored-C Cervical Interbody Fusion System (Dec 28, 2020)

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