# Arthro Kinetics, Inc.

- Location (FDA's records): North Attleboro, MA
- FDA decisions: 2 (2006–2007): 2 510(k) clearances
- Product codes: HRX (2)
- Predicates its devices cite: 4 (0 its own); citations of its devices by later devices: 4 (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
- Endius, Inc.: 1 (https://510kreport.com/company/endius)
- Henke-Sass, Wolf GmbH: 1 (https://510kreport.com/company/henke-sass-wolf)
- Joimax GmbH: 1 (https://510kreport.com/company/joimax)
- Oktas: 1 (https://510kreport.com/company/oktas)

## Firms that cite its devices most
- Hoogland Spine Products, GmbH: 2 (https://510kreport.com/company/hoogland-spine-products)
- Asap Endoscopic Products GmbH: 1 (https://510kreport.com/company/asap-endoscopic-products)
- Spine View, Inc.: 1 (https://510kreport.com/company/spine-view)

## Its most-cited devices
- K061246: Endoscopic Spine System (2006), cited by 4

## Recent decisions
- K070874: Arthro Kinetics Vesalius MR Generator, Models 2004-2006; Accessories for MR Generator (Nov 2, 2007)
- K061246: Endoscopic Spine System (Aug 23, 2006)

Source page: https://510kreport.com/company/arthro-kinetics