Dyna-Tek Industries
Country not established
- Devices
- 2
What Dyna-Tek Industries makes
Dyna-Tek Industries manufactures DE-TOX CONTROL 1 and DE-TOX CONTROL 19, which are likely single-use control devices for monitoring or validating detoxification systems, and DE-TOX TUBES A and B, which appear to be disposable tubing components used in detoxification or filtration processes.
These products are classified as Class I medical devices under FDA regulations and are listed in the FDA 510(k) registry. The company is based in the United States.
Catalogue
De-Tox Control 1 And De-Tox Control 19 Ref K964771
510(k) 510(k)De-Tox Tubes A And De-Tox Tubes B Ref K904326
510(k) 510(k)
Frequently asked questions
How many devices does Dyna-Tek Industries have in the registry?
The registry currently lists 2 devices for Dyna-Tek Industries. Devices recorded under merged duplicate company entries are counted once.
Which registries list Dyna-Tek Industries's devices?
Among its 2 most recently registered devices, Dyna-Tek Industries has devices listed in FDA 510(k) (2 devices).
What risk classes do Dyna-Tek Industries's devices fall under?
Among its 2 most recently registered devices, the classes recorded for Dyna-Tek Industries's devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Dyna-Tek Industries in the registry?
The most recently registered devices listed for Dyna-Tek Industries include DE-TOX CONTROL 1 AND DE-TOX CONTROL 19 and DE-TOX TUBES A AND DE-TOX TUBES B.