# Alexandria Research Technologies, LLC

- Location (FDA's records): Plymouth, MN
- FDA decisions: 2 (2009–2010): 2 510(k) clearances
- Product codes: HSX (2)
- Predicates its devices cite: 5 (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
- DePuy Orthopaedics, Inc.: 2 (https://510kreport.com/company/depuy-orthopaedics)
- Wrightmedicaltechnologyinc: 1 (https://510kreport.com/company/wrightmedicaltechnologyinc)
- Smith & Nephew Richards, Inc.: 1 (https://510kreport.com/company/smith-nephew-richards)

## Its most-cited devices
- K090024: TGS Unicompartmental Knee Arthroplasty System (2009), cited by 1

## Recent decisions
- K101206: TGS Unicompartmental Knee Arthroplasty (TGS Uka) Modular Tibia System (Jul 23, 2010)
- K090024: TGS Unicompartmental Knee Arthroplasty System (May 4, 2009)

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