Innoject, Inc.
Country not established
- Devices
- 1
What Innoject, Inc. makes
Innoject, Inc. manufactures auto-injector devices designed for single-use, pre-filled medication delivery, commonly used in emergency or self-administered treatments.
The company’s portfolio is regulated under FDA Class II devices, with products authorised via the 510(k) pathway. The devices are listed in the FDA’s 510(k) registry.
Catalogue
Innoject Auto-Injector Ref K042557
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Innoject, Inc. have in the registry?
The registry currently lists 1 device for Innoject, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Innoject, Inc.'s devices?
Among its 1 most recently registered device, Innoject, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Innoject, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Innoject, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Innoject, Inc. in the registry?
The most recently registered devices listed for Innoject, Inc. include INNOJECT AUTO-INJECTOR.