# RhythMedix, LLC

- Location (FDA's records): Mt. Laurel, NJ
- FDA decisions: 3 (2014–2026): 3 510(k) clearances
- Product codes: QYX (2), DXH (1)
- Predicates its devices cite: 5 (2 its own); citations of its devices by later devices: 5 (2 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
- iRhythm Technologies, Inc.: 1 (https://510kreport.com/company/irhythm-technologies)
- Mega Electronics, Ltd.: 1 (https://510kreport.com/company/mega-electronics)
- Universal Medical, Inc.: 1 (https://510kreport.com/company/universal-medical)

## Firms that cite its devices most
- Cardiomedix, Inc.: 1 (https://510kreport.com/company/cardiomedix)
- VivaQuant, Inc.: 1 (https://510kreport.com/company/vivaquant)
- Biotricity: 1 (https://510kreport.com/company/biotricity)

## Its most-cited devices
- K141813: Rhythmstar System (2014), cited by 4
- K233584: RhythmStar System (2024), cited by 1

## Recent decisions
- K250793: RhythmStar System (SL) (Apr 21, 2026)
- K233584: RhythmStar System (Jul 8, 2024)
- K141813: Rhythmstar System (Aug 5, 2014)

Source page: https://510kreport.com/company/rhythmedix