Karma Mobility Co, Ltd.
ThailandFDA 510(k) applicant, unverified FDA
- Devices
- 2
- Registrations
- FDA
- FDA recalls
- 0
At a glance
Market reach
- United States
- FDA establishment
What Karma Mobility Co, Ltd. makes
Karma Mobility Co, Ltd. manufactures the Flexx Junior, a Class I medical device designed for pediatric use, available in models FLX-J00 and FLX-J50.
The Flexx Junior is regulated under the FDA’s 510(k) pathway as a Class I device and is listed in the FDA’s 510(k) database. The company is based in the United States.
Catalogue
- GUDID
Flexx Junior (FLX-J00, FLX-J50) Ref K250576
510(k) 510(k)
FDA establishments
- Karma Mobility Co Ltd Amphur Khamtaleso Nakhon Ratchasima · TH FEI 3007675960
Frequently asked questions
How many devices does Karma Mobility Co, Ltd. have in the registry?
The registry currently lists 2 devices for Karma Mobility Co, Ltd.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Karma Mobility Co, Ltd.'s devices?
Among its 2 most recently registered devices, Karma Mobility Co, Ltd. has devices listed in FDA 510(k) (1 device) and FDA GUDID (1 device). A device can be listed in more than one registry, so these counts overlap.
What risk classes do Karma Mobility Co, Ltd.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for Karma Mobility Co, Ltd.'s devices are Class I and Class II. Each device page shows its own class and authorisation.
What are the newest devices from Karma Mobility Co, Ltd. in the registry?
The most recently registered devices listed for Karma Mobility Co, Ltd. include Karma KP-40 and Flexx Junior (FLX-J00, FLX-J50).
Which FDA establishments are linked to Karma Mobility Co, Ltd.?
1 FDA establishment is linked to Karma Mobility Co, Ltd. in the registry; they are listed on the company page.