Dakota Laboratories, Inc.
Country not established
- Devices
- 1
What Dakota Laboratories, Inc. makes
Dakota Laboratories, Inc. makes custom in-the-ear and in-the-canal devices.
The company's portfolio is regulated as Class I devices and is listed in the FDA 510(k) registry, with the company based in the US.
Catalogue
Di Custom In The Ear And In The Canal Ref K920657
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Dakota Laboratories, Inc. have in the registry?
The registry currently lists 1 device for Dakota Laboratories, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Dakota Laboratories, Inc.'s devices?
Among its 1 most recently registered device, Dakota Laboratories, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Dakota Laboratories, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Dakota Laboratories, Inc.'s devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Dakota Laboratories, Inc. in the registry?
The most recently registered devices listed for Dakota Laboratories, Inc. include DI CUSTOM IN THE EAR AND IN THE CANAL.