Mart Tiller Corp.
TaiwanFDA applicant, unverified
- Devices
- 1
What Mart Tiller Corp. makes
Mart Tiller Corp. manufactures the SUPER SOOTHER, a Class II medical device designed for pediatric pain and anxiety management in clinical settings.
The device is regulated under FDA 510(k) clearance as a Class II product and is listed in the U.S. regulatory database. The company is based in the United States.
Catalogue
Super Soother Ref K991914
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Mart Tiller Corp. have in the registry?
The registry currently lists 1 device for Mart Tiller Corp.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Mart Tiller Corp.'s devices?
Among its 1 most recently registered device, Mart Tiller Corp. has devices listed in FDA 510(k) (1 device).
What risk classes do Mart Tiller Corp.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Mart Tiller Corp.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Mart Tiller Corp. in the registry?
The most recently registered devices listed for Mart Tiller Corp. include SUPER SOOTHER.