Aidera AB
SE Last updated 22 Oct 2026
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- Devices
- 2
- Registries
- FDA 510(k)
- FDA recalls
- 0
Catalogue
Aidera Diasend System Ref K101806
Aidera Diasend Ref K083221
What Aidera AB makes
Aidera AB makes the Aidera Diasend System and the Aidera Diasend, which are diabetes management devices used for collecting, analyzing, and reporting glucose data from monitoring devices.
These devices are classified as Class II medical devices and are listed in the FDA 510(k) registry; the company is based in the United States.
Frequently asked questions
What does Aidera AB make?
Aidera AB makes the Aidera Diasend System and the Aidera Diasend, which are diabetes management devices used for collecting, analyzing, and reporting glucose data from monitoring devices.
Where is Aidera AB based?
Aidera AB is based in the United States, as stated in the company's country information.
Which regulatory registry lists Aidera AB's devices?
Aidera AB's devices are listed in the FDA 510(k) registry, which is indicated in the LISTED IN field of the device data.
How are Aidera AB's devices classified?
Aidera AB's devices are classified as Class II medical devices, as specified in the DEVICE CLASSES field.
Information
- Country
- SE