Trans World Agency, Inc.
United StatesFDA applicant, unverified
- Devices
- 2
What Trans World Agency, Inc. makes
Trans World Agency, Inc. manufactures KORICLEAN devices and air mattresses.
These products are classified as Class II medical devices and are listed in the FDA 510(k) registry. The company is based in the United States.
Catalogue
Koriclean Ref K812176
Regimes: 510(k) Registry: 510(k)Air Mattress Ref K813407
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Trans World Agency, Inc. have in the registry?
The registry currently lists 2 devices for Trans World Agency, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Trans World Agency, Inc.'s devices?
Among its 2 most recently registered devices, Trans World Agency, Inc. has devices listed in FDA 510(k) (2 devices).
What risk classes do Trans World Agency, Inc.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for Trans World Agency, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Trans World Agency, Inc. in the registry?
The most recently registered devices listed for Trans World Agency, Inc. include KORICLEAN and AIR MATTRESS.