# Arthromeda, Inc.

- Location (FDA's records): Lowell, MA
- FDA decisions: 1 (2014–2014): 1 510(k) clearance
- Product codes: LLZ (1)
- Predicates its devices cite: 2 (0 its own); citations of its devices by later devices: 0 (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
- Merdian Technique, Ltd.: 1 (https://510kreport.com/company/merdian-technique)
- Agfa Healthcare N.V.: 1 (https://510kreport.com/company/agfa-healthcare)

## Recent decisions
- K142944: ArthroPlan Digital Templating Software (Dec 16, 2014)

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