Identity
- Trade Name
- LNX Floating CM Legrest (Upper Assy) FDA UDI
- Generic Name
- Wheelchair footrest/legrest FDA UDI
- Device Name
- Upper Floating Center Mount Legrest Assembly. Assembly includes actuator motor. Optional wheelchair component designed for use with Motion Concepts power positioning systems. FDA UDI
- Model / Reference
- D-0101-LNXFFP FDA UDI
- Description
- Upper Floating Center Mount Legrest Assembly. Assembly includes actuator motor. Optional wheelchair component designed for use with Motion Concepts power positioning systems. FDA UDI
Identifiers
- Catalog Number
- LNXFFP FDA UDI
- Primary DI / UDI-DI
- 07540147002343 FDA UDI
- FDA Product Code
- KNN FDA UDI
- GMDN Term
- Wheelchair footrest/legrest FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 890.3920 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
No
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
Yes
FDA UDI
Lot / Batch Number
No
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
Yes
FDA UDI
Category: Wheelchair footrest/legrest
LNX Floating CM Legrest (Upper Assy) by Motion Concepts Inc — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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Also classified as Wheelchair footrest/legrest.
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- Drive — Drive Devilbiss Healthcare · Class I
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 I | Pending data |
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Manufacturer
- Manufacturer
- Motion Concepts Inc
Sources (1)
- FDA UDI 544a3cbb-e9b7-4732-a0fe-04402620f91e 35 fields · synced May 30, 2026