Identity
- Trade Name
- KneeKG system FDA UDI
- Generic Name
- Gait analysis system FDA UDI
- Model / Reference
- 0 FDA UDI
Identifiers
- Catalog Number
- P-142 FDA UDI
- Primary DI / UDI-DI
- 00627843933236 FDA UDI
- 510(k) Number
- K091000 FDA UDI
- FDA Product Code
- LXJ FDA UDI
- GMDN Term
- Gait analysis system FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 890.5360 FDA UDI
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
No
FDA UDI
Single Use
No
FDA UDI
Implantable
No
FDA UDI
Contains Latex
No
FDA UDI
Prescription Use
Yes
FDA UDI
Over-the-Counter
No
FDA UDI
Convenience Kit
No
FDA UDI
Combination Product
No
FDA UDI
HCT/P
No
FDA UDI
Premarket Exempt
No
FDA UDI
Lot / Batch Number
No
FDA UDI
Serial Number
Yes
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
Yes
FDA UDI
Category: Gait analysis system
KneeKG system by Emovi Inc — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Gait analysis system.
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- FDM-SX System — zebris MEDICAL GmbH · Class I
- Kinesis QTUG — KINESIS · Class I
- VICON — VICON MOTION SYSTEMS INC · Class II
Authorization Coverage (1 country)
Regulatory Authorizations
United States Pending data
FDA UDI
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class II | Pending data |
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Manufacturer
- Manufacturer
- Emovi Inc
Sources (1)
- FDA UDI 6c0e25be-c6bb-4e18-ab7d-fd1633eb9b6a 34 fields · synced May 30, 2026