Dymedix, Inc.
United StatesFDA 510(k) applicant, unverified
- Devices
- 4
What Dymedix, Inc. makes
Dymedix, Inc. manufactures respiratory and limb movement sensors, including reusable models for monitoring breathing effort and airflow, as well as chin electrodes for sleep-related applications. The company also produces sensors designed to detect snoring and limb activity, primarily for use in respiratory and sleep diagnostics.
These devices are classified as Class II under FDA regulations and are listed via the 510(k) pathway. The company is based in the United States.
Catalogue
- 510(k) 510(k)
Chin Electrode Ref K020468
510(k) 510(k)- 510(k) 510(k)
Dymedix Reusable Airflow/Snore Sensor Ref K040069
510(k) 510(k)
Frequently asked questions
How many devices does Dymedix, Inc. have in the registry?
The registry currently lists 4 devices for Dymedix, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Dymedix, Inc.'s devices?
Among its 4 most recently registered devices, Dymedix, Inc. has devices listed in FDA 510(k) (4 devices).
What risk classes do Dymedix, Inc.'s devices fall under?
Among its 4 most recently registered devices, the classes recorded for Dymedix, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Dymedix, Inc. in the registry?
The most recently registered devices listed for Dymedix, Inc. include RESPIRATORY BELT SENSOR, MODEL 6000S; LIMB MOVEMENT SENSOR, MODEL 3000S, CHIN ELECTRODE, DYMEDIX REUSABLE RESPIRATORY EFFORT BELT SENSOR, MODEL 6015 AND DYMEDIX REUSABLE LIMB MOVEMENT SENSOR, MODEL 3100 and DYMEDIX REUSABLE AIRFLOW/SNORE SENSOR.