FEI 3005905321
Ki Mobility
5201 WOODWARD DR, Stevens Point, WI, US
MDR events38All time
Recalls1All time
Registered products8
Establishment typeManufactureManufacture Medical Device
Registered product codes
8 product codes
Recent MDR events
38 on file
- KIJul 21, 2026Injury3005905321-2026-00006
- KIJul 21, 2026Injury3005905321-2026-00007
- KIJul 21, 2026Malfunction3005905321-2026-00009
- KIJul 21, 2026Injury3005905321-2026-00008
- KIFeb 18, 2026Malfunction3005905321-2026-00003
- KIFeb 18, 2026Malfunction3005905321-2026-00004
- KIFeb 18, 2026Malfunction3005905321-2026-00005
- KIFeb 3, 2026Injury3005905321-2026-00001
- KI MOBILITY, LLCNov 21, 2025Malfunction3005905321-2025-00007
- KI MOBILITY, LLCAug 29, 2025Malfunction3005905321-2025-00006
Compliance history
Matched by FEI 3005905321.
FDA inspections
2 on file
- Voluntary Action Indicated (VAI)Sep 19, 2025
Compliance: Devices · Citations posted
- No Action Indicated (NAI)Sep 19, 2025
Postmarket Assurance: Devices · Citations posted
Inspection citations
2 on file
Top cited requirements
Compare to industry ↗- 21 CFR 820.100(a)Sep 19, 2025
Lack of or inadequate procedures
- 21 CFR 820.198(a)Sep 19, 2025
Lack of or inadequate complaint procedures
Compliance actions
0 on file
No warning letters or injunctions on file for this FEI number.
Import refusals
0 on file
No import refusals on file for this FEI number.