# Scient'X USA, Inc.

- Location (FDA's records): Round Rock, TX
- FDA decisions: 4 (2003–2009): 4 510(k) clearances
- Product codes: MNH (1), MAX (1), KWQ (1), MQP (1)
- Predicates its devices cite: 2 (0 its own); citations of its devices by later devices: 7 (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
- Abbott Spine, Inc.: 1 (https://510kreport.com/company/abbott-spine)
- Scient'X: 1 (https://510kreport.com/company/scient-x)

## Firms that cite its devices most
- Qualgenix: 2 (https://510kreport.com/company/qualgenix)
- Musculoskeletal Clinical Regulatory Advisers: 1 (https://510kreport.com/company/musculoskeletal-clinical-regulatory-advisers)
- Spineway: 1 (https://510kreport.com/company/spineway)
- Camber Spine Technologies: 1 (https://510kreport.com/company/camber-spine-technologies)
- Icotec AG: 1 (https://510kreport.com/company/icotec)
- Eit Emerging Implant Technologies GmbH: 1 (https://510kreport.com/company/eit-emerging-implant-technologies)

## Its most-cited devices
- K080588: Scient'x Tribeca VBR (2008), cited by 7

## Recent decisions
- K081548: Anterior Buttress Plate (Jan 29, 2009)
- K080588: Scient'x Tribeca VBR (May 30, 2008)
- K053292: Davantis/Antelys Vertebral Body Replacements (Jan 19, 2006)
- K031290: Modification to Easys Transverse Connection (May 13, 2003)

Source page: https://510kreport.com/company/scient-x-usa