Felton International, Inc.
United StatesFDA applicant, unverified
- Devices
- 2
What Felton International, Inc. makes
Felton International, Inc. makes needle-free injector systems and human subcutaneous injectors, including the BI-3M Needle-Free Injector System and the Human Subcutaneous Injector, Model HSI 500.
These devices 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
Bi-3M Needle-Free Injector System Ref K013256
Regimes: 510(k) Registry: 510(k)Human Subcutaneous Injector, Model Hsi 500 Ref K041280
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Felton International, Inc. have in the registry?
The registry currently lists 2 devices for Felton International, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Felton International, Inc.'s devices?
Among its 2 most recently registered devices, Felton International, Inc. has devices listed in FDA 510(k) (2 devices).
What risk classes do Felton International, Inc.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for Felton International, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Felton International, Inc. in the registry?
The most recently registered devices listed for Felton International, Inc. include BI-3M NEEDLE-FREE INJECTOR SYSTEM and HUMAN SUBCUTANEOUS INJECTOR, MODEL HSI 500.