Facility

WHILL, INC.

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

Key facts

1recalls · worst Class I

—inspections in our data

—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)	3021071770
Establishment type	Develop Specifications But Do Not Manufacture At This Facility
Location	2-1-11 Higashi-Shinagawa Shinagawa-ku Tokyo, JP 14000
Registration status	Active · expires 2026
Parent company	WHILL, Inc. (owner-operator 10083588)

Activity by year

Recalls (1)

Devices registered here (1)

Accessories, Wheelchair
Product code KNO (opens in a new tab) · Class I · Physical Medicine · 21 CFR 890.3910

Recalls & enforcement

Class IOngoing2025-12-29
Cyber vulnerability of BLE communication was found by CISA VDP program.

All facilities operated by WHILL, Inc.

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. “WHILL, INC. (FEI 3021071770) — FDA facility record.” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/facility/3021071770-whill-inc/

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