KINVENT Sens V2R01
KINVENT Sens V2R01 is an electronic goniometer/kinesiology sensor (FDA Class I; FDA product code KQX, Goniometer, Ac-Powered) made by Kinvent Hellas, listed in FDA GUDID since 1 Aug 2020 (UDI-DI 03770011995554), 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 | Number03770011995554 | Date1 Aug 2020 | StatusListed |
Official records
- AccessGUDID record 03770011995554
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — GUDID listing Listed
Specification
- Trade name
- Kinvent
- Generic name
- Electronic goniometer/kinesiology sensor
- Model / reference
- Sens V2R01
- Description
- Sens is an inertial sensor to measure the range of motion and to compare the symmetry between the injured limb’s amplitude and the healthy limb.
- Primary DI / UDI-DI
- 03770011995554
- FDA product code
- KQX
- GMDN term
- Electronic goniometer/kinesiology sensor
- Device class
- Class I
- Regulation number
- 888.1500
- GUDID distribution status
- In Commercial Distribution
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