# Dymedix, Inc.

- Location (FDA's records): Stoughton, WI
- FDA decisions: 4 (2000–2004): 4 510(k) clearances
- Product codes: BZQ (2), GXY (1), MNR (1)
- Predicates its devices cite: 6 (1 its own); citations of its devices by later devices: 3 (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
- Pro-Tech, Inc.: 3 (https://510kreport.com/company/pro-tech)
- Medicotest, Inc.: 1 (https://510kreport.com/company/medicotest)
- Alphamed, Inc.: 1 (https://510kreport.com/company/alphamed)

## Firms that cite its devices most
- Hidalgo Limited: 2 (https://510kreport.com/company/hidalgo)

## Its most-cited devices
- K040605: Dymedix Reusable Respiratory Effort Belt Sensor, Model 6015 and Dymedix Reusable Limb Movement Sensor, Model 3100 (2004), cited by 2
- K001030: Respiratory Belt Sensor, Model 6000S; Limb Movement Sensor, Model 3000S (2000), cited by 1

## Recent decisions
- K040069: Dymedix Reusable Airflow/Snore Sensor (May 5, 2004)
- K040605: Dymedix Reusable Respiratory Effort Belt Sensor, Model 6015 and Dymedix Reusable Limb Movement Sensor, Model 3100 (Apr 26, 2004)
- K020468: Chin Electrode (Apr 16, 2002)
- K001030: Respiratory Belt Sensor, Model 6000S; Limb Movement Sensor, Model 3000S (May 11, 2000)

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