Tympany, Inc.
United StatesFDA 510(k) applicant, unverified
- Devices
- 2
What Tympany, Inc. makes
Tympany, Inc. makes medical devices such as OTOGRAM and CA3350, which are types of otogram devices.
The company's portfolio is regulated as Class II devices and is listed in the FDA 510(k) registry, with the company based in the US.
Catalogue
Otogram, CA3350 Ref K070118
510(k) 510(k)Otogram Ref K041853
510(k) 510(k)
Frequently asked questions
How many devices does Tympany, Inc. have in the registry?
The registry currently lists 2 devices for Tympany, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Tympany, Inc.'s devices?
Among its 2 most recently registered devices, Tympany, Inc. has devices listed in FDA 510(k) (2 devices).
What risk classes do Tympany, Inc.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for Tympany, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Tympany, Inc. in the registry?
The most recently registered devices listed for Tympany, Inc. include OTOGRAM, CA3350 and OTOGRAM.