# Myotronics-Noromed, Inc.

- Location (FDA's records): Tukwila, WA
- FDA decisions: 7 (1999–2011): 7 510(k) clearances
- Product codes: HCC (3), NUW (2), KZM (2)
- Predicates its devices cite: 11 (3 its own); citations of its devices by later devices: 8 (3 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
- Myo-Tronics Research, Inc.: 3 (https://510kreport.com/company/myo-tronics-research)
- Lead-Lok, Inc.: 1 (https://510kreport.com/company/lead-lok)
- Uni-Patch, Inc.: 1 (https://510kreport.com/company/uni-patch)
- Vermont Medical, Inc.: 1 (https://510kreport.com/company/vermont-medical)
- Noromed, Inc.: 1 (https://510kreport.com/company/noromed)
- Myo-Tronics, Inc.: 1 (https://510kreport.com/company/myo-tronics)

## Firms that cite its devices most
- Medotech A/S: 1 (https://510kreport.com/company/medotech-a-s)
- Ito Co., Ltd.: 1 (https://510kreport.com/company/ito)
- Lorenz Biotech S.P.A.: 1 (https://510kreport.com/company/lorenz-biotech)
- Neuromuscular Technologies, Inc.: 1 (https://510kreport.com/company/neuromuscular-technologies)
- S.L.P., Ltd.: 1 (https://510kreport.com/company/slp)

## Its most-cited devices
- K031998: Model J-5 Mvo-Monitor (2003), cited by 4
- K013399: Model Mes-9000/Emg System (2001), cited by 2
- K992694: Modification to K6-I Diagnostic System, Model K6-I (1999), cited by 1
- K992439: Norodyn 8000 Semg System, ND-8000 (1999), cited by 1

## Recent decisions
- K111687: Emg System (Sep 29, 2011)
- K040400: Myo-Trode SG Disposable Electrode (Jul 20, 2004)
- K031998: Model J-5 Mvo-Monitor (Jul 24, 2003)
- K013399: Model Mes-9000/Emg System (Nov 13, 2001)
- K003287: Model K7 Evaluation Device (Nov 6, 2000)
- K992694: Modification to K6-I Diagnostic System, Model K6-I (Sep 10, 1999)
- K992439: Norodyn 8000 Semg System, ND-8000 (Aug 13, 1999)

Source page: https://510kreport.com/company/myotronics-noromed