Iaid
South KoreaFDA applicant, unverified
- Devices
- 1
What Iaid makes
Iaid manufactures the Aid-U, a medical device designed for urinary incontinence management, providing intermittent catheterization support for patients.
The Aid-U is classified as a Class II device under FDA regulations and is listed via the 510(k) pathway. The company is based in the United States.
Catalogue
Aid-U Ref K231662
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Iaid have in the registry?
The registry currently lists 1 device for Iaid. Devices recorded under merged duplicate company entries are counted once.
Which registries list Iaid's devices?
Among its 1 most recently registered device, Iaid has devices listed in FDA 510(k) (1 device).
What risk classes do Iaid's devices fall under?
Among its 1 most recently registered device, the classes recorded for Iaid's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Iaid in the registry?
The most recently registered devices listed for Iaid include Aid-U.