# Sanacor

- Location (FDA's records): American Fork, UT
- FDA decisions: 3 (2007–2009): 3 510(k) clearances
- Product codes: MNH (2), KWQ (1)
- Predicates its devices cite: 13 (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
- Signus Medizintechnik GmbH: 2 (https://510kreport.com/company/signus-medizintechnik)
- Alphaspine, Inc.: 1 (https://510kreport.com/company/alphaspine)
- Synthes (Usa): 1 (https://510kreport.com/company/synthes-usa)
- Depuy Motech Acromed: 1 (https://510kreport.com/company/depuy-motech-acromed)
- Medicrea Technologies: 1 (https://510kreport.com/company/medicrea-technologies)
- Biomedical Enterprises, Inc.: 1 (https://510kreport.com/company/biomedical-enterprises)
- Pioneer Surgical Technology: 1 (https://510kreport.com/company/pioneer-surgical-technology)
- Spinal Concepts, Inc.: 1 (https://510kreport.com/company/spinal-concepts)

## Firms that cite its devices most
- Pioneer Surgical Technology: 2 (https://510kreport.com/company/pioneer-surgical-technology)
- Nexus Spine, LLC: 1 (https://510kreport.com/company/nexus-spine)

## Its most-cited devices
- K070933: Lowtop Pedicle Screw System (2007), cited by 2
- K090477: Alpine Pedicle Screw System (2009), cited by 1

## Recent decisions
- K090477: Alpine Pedicle Screw System (Jul 27, 2009)
- K073500: Active Anterior Cervical Plate System (Jul 3, 2008)
- K070933: Lowtop Pedicle Screw System (Jun 13, 2007)

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