# Mdpo, LLC

- Location (FDA's records): Alexandria, VA
- FDA decisions: 1 (2010–2010): 1 510(k) clearance
- Product codes: KTT (1)
- Predicates its devices cite: 6 (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
- Richards Medical Co., Inc.: 1 (https://510kreport.com/company/richards-medical)
- Smith & Nephew Richards, Inc.: 1 (https://510kreport.com/company/smith-nephew-richards)
- Smith & Nephew, Inc.: 1 (https://510kreport.com/company/smith-nephew)
- DePuy Orthopaedics, Inc.: 1 (https://510kreport.com/company/depuy-orthopaedics)
- Biomet Manufacturing Corp: 1 (https://510kreport.com/company/biomet-manufacturing)
- Ebi, L.P.: 1 (https://510kreport.com/company/ebi)

## Recent decisions
- K093753: Mdpo Frame System (Aug 26, 2010)

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