# Guidemia Technologies, LLC

- Location (FDA's records): Los Alamitos, CA
- FDA decisions: 2 (2012–2017): 2 510(k) clearances
- Product codes: PNN (1), LLZ (1)
- Predicates its devices cite: 0 (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

## Recent decisions
- K162850: GuideMia Ortho+ (Mar 24, 2017)
- K121466: Guidemia (May 31, 2012)

Source page: https://510kreport.com/company/guidemia-technologies