# Mx Orthopedics, Corp.

- Location (FDA's records): Lexington, MA
- FDA decisions: 4 (2015–2017): 4 510(k) clearances
- Product codes: JDR (2), HWC (1), HRS (1)
- 510(k) review time since 2016: median 108 days, against 122 for FDA's reviews in the same codes and years (2 of 3 faster)
- Predicates its devices cite: 11 (1 its own); citations of its devices by later devices: 5 (1 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
- Biomedical Ent., Inc.: 4 (https://510kreport.com/company/biomedical-ent)
- Synthes (Usa): 2 (https://510kreport.com/company/synthes-usa)
- Newdeal Sas: 2 (https://510kreport.com/company/newdeal)
- Wrightmedicaltechnologyinc: 1 (https://510kreport.com/company/wrightmedicaltechnologyinc)
- Biomedical Enterprises, Inc.: 1 (https://510kreport.com/company/biomedical-enterprises)

## Firms that cite its devices most
- Activortho, Inc.: 2 (https://510kreport.com/company/activortho)
- Arthrex, Inc.: 2 (https://510kreport.com/company/arthrex)

## Its most-cited devices
- K160427: dynaMX (TM) Nitinol Compression Screw (2016), cited by 2
- K143622: dynaMX Compression Staple (2015), cited by 1
- K153129: dynaMX Tabbed Staple (2016), cited by 1
- K161303: dynaMX™ Compression Plate (2017), cited by 1

## Recent decisions
- K161303: dynaMX™ Compression Plate (Jan 26, 2017)
- K160427: dynaMX (TM) Nitinol Compression Screw (Jun 3, 2016)
- K153129: dynaMX Tabbed Staple (Jan 28, 2016)
- K143622: dynaMX Compression Staple (Jun 17, 2015)

Source page: https://510kreport.com/company/mx-orthopedics