# Medi USA, LP

- Location (FDA's records): Whitsett, NC
- FDA decisions: 4 (1994–2022): 4 510(k) clearances
- Product codes: JOW (2), DWL (2)
- Predicates its devices cite: 2 (1 its own); citations of its devices by later devices: 2 (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
- Devon Medical, Inc.: 1 (https://510kreport.com/company/devon-medical)

## Firms that cite its devices most
- Manamed, Inc.: 1 (https://510kreport.com/company/manamed)

## Its most-cited devices
- K183631: medi pneumatic compression system (pcs) – brio (Model 651) (2019), cited by 2

## Recent decisions
- K221654: medi pneumatic compression system (pcs)-genius (Model 652) (Jul 7, 2022)
- K183631: medi pneumatic compression system (pcs) – brio (Model 651) (Jan 25, 2019)
- K051324: Medi Butler (Dec 5, 2005)
- K941926: Medi Strumpf (Jun 15, 1994)

Source page: https://510kreport.com/company/medi-usa