ActivForce 2 ActivM2
by Activbody
ActivForce 2 ActivM2 is an electronic goniometer/kinesiology sensor (FDA Class II) made by Activbody, listed in FDA GUDID since 14 Sep 2026 (UDI-DI 00850004866320), registry data as of 23 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 | Number00850004866320 | Date14 Sep 2026 | StatusListed |
Official records
- AccessGUDID record 00850004866320
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — GUDID listing Listed
Specification
- Trade name
- ActivForce 2
- Generic name
- Electronic goniometer/kinesiology sensor
- Model / reference
- ActivM2
- Primary DI / UDI-DI
- 00850004866320
- FDA product code
- LBB, KQX
- GMDN term
- Electronic goniometer/kinesiology sensor
- Device class
- Class II
- Regulation number
- 888.1240, 888.1500
- GUDID distribution status
- In Commercial Distribution
- MRI safety
- MR Unsafe
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