# Midwest Reprocessing Center, LLC

- Location (FDA's records): Birmingham, AL
- FDA decisions: 4 (2010–2011): 4 510(k) clearances
- Product codes: JOW (2), NMD (1), NLF (1)
- Predicates its devices cite: 46 (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
- Hygia Health Services, Inc.: 12 (https://510kreport.com/company/hygia-health-services)
- Compression Therapy Concepts, Inc.: 6 (https://510kreport.com/company/compression-therapy-concepts)
- Somanetics Corp.: 6 (https://510kreport.com/company/somanetics)
- Microtek Medical, Inc.: 4 (https://510kreport.com/company/microtek-medical)
- Advanced Instruments, Inc.: 2 (https://510kreport.com/company/advanced-instruments)
- Huntleigh Technology, Inc.: 2 (https://510kreport.com/company/huntleigh-technology)
- Kci New Technologies, Inc.: 2 (https://510kreport.com/company/kci-new-technologies)
- Kinetic Concepts, Inc.: 2 (https://510kreport.com/company/kinetic-concepts)

## Recent decisions
- K111007: Midwest Reprocessing Center Reprocessed LNCS Sessors; Midwest Reprocessing Center Reprocessed Oximax Sensors; Midwest RE (Jun 8, 2011)
- K101280: Midwestern Reprocessing Center Reprocessed Pulse Oximeter Probe (Oct 7, 2010)
- K101702: Midwest Reprocessing Center Reprocessed Venodyne Sleeves/Foot Cuffs (Aug 27, 2010)
- K101330: Midwest Reprocessing Center Reprocessed SCD Express Sleeves/ Foot Cuffs, Midwest Reprocessing Center Reprocessed Alp Sle (Aug 27, 2010)

Source page: https://510kreport.com/company/midwest-reprocessing-center