Facility

Ki Mobility

1 recall(s) on record — most severe on record: Class III.

Key facts

1recalls · worst Class III

1inspections · worst VAI

—warning letters in our data

Recalls are listed for the parent company: openFDA recall records do not name a facility. How we attribute records

FDA Establishment Identifier (FEI)	3005905321
Establishment type	Repack or Relabel Medical Device; Develop Specifications But Do Not Manufacture At This Facility; Manufacture Medical Device
Location	5201 WOODWARD DR Stevens Point, WI, US 54481
Registration status	Active · expires 2026
Parent company	Ki Mobility (owner-operator 10023866)
Brand names	Axiom PXALCL; Axiom Back AXLB; Axiom PXPL; Axiom Back AXPL; Axiom Custom Back AXCB; Axiom PXAL; Axiom Back AXPB; Sentinel; Axiom Back AXDL; Axiom Custom Seating

Activity by year

Recalls (1)
Inspections (1)

Devices registered here (1)

Components, Wheelchair
Product code KNN (opens in a new tab) · Class I · Physical Medicine · 21 CFR 890.3920

Recalls & enforcement

Class IIITerminated2021-11-19
The Instructions for Use provided with the device contained information intended for use of a mechanical wheelchair, not a chair with casters.

FDA inspections (1)

VAI2025-09-19
Voluntary Action Indicated · Compliance: Devices; Postmarket Assurance: Devices · citations posted

Source: U.S. FDA Inspections Dashboard (opens in a new tab) (device inspection classifications, 2016–present). Data as of 2026-10-06. The dashboard profile can take several seconds to load.

All facilities operated by Ki Mobility

Source: U.S. FDA via openFDA (opens in a new tab) (device registration & enforcement). Data as of 2026-10-06. Verify this facility record at FDA → (opens in a new tab)

Cite this record

RegWarden. “Ki Mobility (FEI 3005905321) — FDA facility record.” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/facility/3005905321-ki-mobility/

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