# Ortho Kinematics, Inc.

- Location (FDA's records): Washington, DC
- FDA decisions: 6 (2011–2017): 6 510(k) clearances
- Product codes: LLZ (6)
- 510(k) review time since 2016: median 33 days, against 107 for FDA's reviews in the same codes and years (3 of 3 faster)
- Predicates its devices cite: 9 (4 its own); citations of its devices by later devices: 5 (4 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
- Medical Metrics, Inc.: 2 (https://510kreport.com/company/medical-metrics)
- STERIS Corporation: 2 (https://510kreport.com/company/steris)
- Nemaris, Inc.: 1 (https://510kreport.com/company/nemaris)

## Firms that cite its devices most
- Ib Lab GmbH: 1 (https://510kreport.com/company/ib-lab)

## Its most-cited devices
- K133875: The Kinegraph Vma (Vertebral Motion Analyzer) Software Version 2.2, the Motion Normalizer Patient Handling and Data (2014), cited by 1
- K171617: OKI Surgical Planning Software (2017), cited by 1
- K130743: The Kinegraph Vma (Vertebral Motion Analyzer) Software Version 2.0; the Motion Normalizer Patient Handling and Data Coll (2013), cited by 1
- K112109: The Kinegraph Vma Software, the Motion Normalizer Patient Handling and Data Collection Device (2011), cited by 1
- K172327: VMA™ System version 3.0 (2017), cited by 1

## Recent decisions
- K173247: Surgical Planning Software version 1.1 (Nov 8, 2017)
- K172327: VMA™ System version 3.0 (Aug 25, 2017)
- K171617: OKI Surgical Planning Software (Aug 22, 2017)
- K133875: The Kinegraph Vma (Vertebral Motion Analyzer) Software Version 2.2, the Motion Normalizer Patient Handling and Data (Jan 17, 2014)
- K130743: The Kinegraph Vma (Vertebral Motion Analyzer) Software Version 2.0; the Motion Normalizer Patient Handling and Data Coll (Aug 6, 2013)
- K112109: The Kinegraph Vma Software, the Motion Normalizer Patient Handling and Data Collection Device (Dec 22, 2011)

Source page: https://510kreport.com/company/ortho-kinematics