Bionik, Inc.
Country not established
Bionik, Inc. is a medical device manufacturer, with 2 devices listed in FDA GUDID (FDA Class I and II) as of 15 Nov 2026.
- Devices
- 2
Registry facts
- Registries
- FDA GUDID 2
- Device classes
- FDA Class I 1
- FDA Class II 1
- Identifiers
- DUNS 080397777
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
- Registry: GUDID
- Registry: GUDID
Company details
- DUNS number
- 080397777
Frequently asked questions
How many devices does BIONIK, INC. have in the registry?
The registry currently lists 2 devices for BIONIK, INC.. Devices recorded under merged duplicate company entries are counted once.
Which registries list BIONIK, INC.'s devices?
Among its 2 most recently registered devices, BIONIK, INC. has devices listed in FDA GUDID (2 devices).
What risk classes do BIONIK, INC.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for BIONIK, INC.'s devices are Class I and Class II. Each device page shows its own class and authorisation.
What are the newest devices from BIONIK, INC. in the registry?
The most recently registered devices listed for BIONIK, INC. include InMotion ARM SE4 and InMotion ARM/HAND SE4HA4.