# Wmi Enterprises, LLC

- Location (FDA's records): Chicago, IL
- FDA decisions: 2 (2010–2010): 2 510(k) clearances
- Product codes: JOW (2)
- Predicates its devices cite: 5 (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
- Thermotek, Inc.: 1 (https://510kreport.com/company/thermotek)
- Aircast, Inc.: 1 (https://510kreport.com/company/aircast)
- Doctors Orders: 1 (https://510kreport.com/company/doctors-orders)
- Hygia Health Services, Inc.: 1 (https://510kreport.com/company/hygia-health-services)
- Huntleigh Technology, Inc.: 1 (https://510kreport.com/company/huntleigh-technology)

## Recent decisions
- K101035: Wmi Reprocessed DVT Wrap, Wmi Reprocessed Thermal Wrap Model: RD-1000F, RD-1000C, RT 2000A, RT 2000B, RT 2000KF, RT 2000 (Oct 29, 2010)
- K100969: Wmi DVT Wrap, Wmi Thermal Wrap Model: D-1000F, D-1000C, T-2000A, T-2000B, T-2000KF, T-2000S, T-2000N (Sep 20, 2010)

Source page: https://510kreport.com/company/wmi-enterprises