InMotion ARM SE4
by Bionik, Inc.
InMotion ARM SE4 is a virtual-display rehabilitation system (FDA Class I) made by Bionik, Inc., listed in FDA GUDID since 4 Oct 2019 (UDI-DI 00860001346701), registry data as of 22 Oct 2026.
Listed
Valid until
Not applicable
FDA recalls
Not checked
Documents
None
Trust
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| United States | GUDID listing | Number00860001346701 | Date4 Oct 2019 | StatusListed |
Official records
- AccessGUDID record 00860001346701
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — GUDID listing Listed
Specification
- Trade name
- InMotion ARM
- Generic name
- Virtual-display rehabilitation system, powered-support, upper-limb
- Model / reference
- SE4
- Primary DI / UDI-DI
- 00860001346701
- FDA product code
- BXB, IKK
- GMDN term
- Virtual-display rehabilitation system, powered-support, upper-limb
- Device class
- Class I
- Regulation number
- 890.5380, 890.1925
- GUDID distribution status
- In Commercial Distribution
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