# Spineup, Inc.

- Location (FDA's records): Hollywood, FL
- FDA decisions: 2 (2022–2025): 2 510(k) clearances
- Product codes: KWQ (1), OVE (1)
- Predicates its devices cite: 7 (0 its own); citations of its devices by later devices: 3 (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
- Astura Medical: 1 (https://510kreport.com/company/astura-medical)
- Dio Medical Co., Ltd.: 1 (https://510kreport.com/company/dio-medical)
- Biomet Spine: 1 (https://510kreport.com/company/biomet-spine)
- Medtronic Sofamor Danek USA, Inc.: 1 (https://510kreport.com/company/medtronic-sofamor-danek-usa)
- Reliance Medical Systems, LLC: 1 (https://510kreport.com/company/reliance-medical-systems)
- Alphatec Spine, Inc.: 1 (https://510kreport.com/company/alphatec-spine)
- Centinel Spine, Inc.: 1 (https://510kreport.com/company/centinel-spine)

## Firms that cite its devices most
- Implanet, S.A.: 1 (https://510kreport.com/company/implanet)
- Artfx Medical: 1 (https://510kreport.com/company/artfx-medical)
- Mikron Makina Sanayi VE Tic. Ltd. Sti.: 1 (https://510kreport.com/company/mikron-makina-sanayi-ve-tic-sti)

## Its most-cited devices
- K212358: Romero Cervical Cage (2022), cited by 3

## Recent decisions
- K250446: Frida™ Anterior Cervical Plate System (May 23, 2025)
- K212358: Romero Cervical Cage (Jan 10, 2022)

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