# Orthoscan, Inc.

- Location (FDA's records): Scottsdale, AZ
- FDA decisions: 6 (2001–2021): 6 510(k) clearances
- Names in FDA's records: Orthoscan, Inc. (5); Orthoscan , Ltd. (1)
- Product codes: OXO (5), KQX (1)
- Predicates its devices cite: 5 (2 its own); citations of its devices by later devices: 9 (2 its own)
- Recalls linked to its devices: 4 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms whose devices it cites most
- Ziehm Imaging GmbH: 1 (https://510kreport.com/company/ziehm-imaging)
- Orthopedic Systems, Inc.: 1 (https://510kreport.com/company/orthopedic-systems)
- Skill Technologies, Inc.: 1 (https://510kreport.com/company/skill-technologies)

## Firms that cite its devices most
- Ziehm-Orthoscan, Inc.: 3 (https://510kreport.com/company/ziehm-orthoscan)
- Hologic, Inc.: 2 (https://510kreport.com/company/hologic)
- Pausch Medical GmbH: 1 (https://510kreport.com/company/pausch-medical)
- Turner Imaging Systems, Inc.: 1 (https://510kreport.com/company/turner-imaging-systems)

## Its most-cited devices
- K113708: Orthoscan Mobile DI Mini C-Arm (2012), cited by 4
- K213113: Orthoscan Tau Mini C-Arm (2021), cited by 2
- K051754: Orthoscan, Orthoscan HD (2005), cited by 1
- K133174: Orthoscan FD Mini C-Arm (2014), cited by 1
- K183220: OrthoScan TAU Mini C-Arm (2019), cited by 1

## Recent decisions
- K213113: Orthoscan Tau Mini C-Arm (Oct 21, 2021)
- K183220: OrthoScan TAU Mini C-Arm (Jun 21, 2019)
- K133174: Orthoscan FD Mini C-Arm (Mar 28, 2014)
- K113708: Orthoscan Mobile DI Mini C-Arm (Jan 5, 2012)
- K051754: Orthoscan, Orthoscan HD (Aug 9, 2005)
- K011827: Ortelius 800 (Aug 28, 2001)

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