# Activortho, Inc.

- Location (FDA's records): Plymouth, MN
- FDA decisions: 2 (2019–2019): 2 510(k) clearances
- Product codes: HWC (2)
- Predicates its devices cite: 7 (1 its own); citations of its devices by later devices: 1 (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
- Mx Orthopedics, Corp.: 2 (https://510kreport.com/company/mx-orthopedics)
- Synthes (Usa): 2 (https://510kreport.com/company/synthes-usa)
- Vilex, LLC: 1 (https://510kreport.com/company/vilex)
- Pioneer Surgical Technology: 1 (https://510kreport.com/company/pioneer-surgical-technology)

## Its most-cited devices
- K181610: ActivOrtho Nitinol Compression Screw System (2019), cited by 1

## Recent decisions
- K191817: ActivOrtho Continuous Compression Screw System (Jul 26, 2019)
- K181610: ActivOrtho Nitinol Compression Screw System (Mar 12, 2019)

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