# Whill, Inc.

> Medical device manufacturer record on deviCERTS, compiled from public registries. Whill, Inc. is a medical device manufacturer based in Japan, with 11 devices listed in EUDAMED, FDA GUDID and FDA 510(k) (EU Class I; FDA Class II) and 2 FDA recalls as of 15 Nov 2026.

- Canonical page: <https://devicerts.com/manufacturers/whill-inc>
- Country: Japan (from SRN)
- EUDAMED actor status: active
- Role: Manufacturer
- Registrations: EUDAMED, FDA
- EUDAMED SRN: JP-MF-000016481
- FDA FEI: 3021071770
- DUNS: 691746455

## Figures

- Devices: 11
- FDA recalls (matched to the firm by name): 2, 2 ongoing

## Registry facts

*Every device of the manufacturer. A device listed in two registries counts in both.*

- Registries: EUDAMED 6, FDA GUDID 4, FDA 510(k) 2
- Device classes: EU Class I 6, FDA Class II 5
- EMDN [Y12 Personal mobility devices](https://devicerts.com/categories/emdn/Y12): 6 devices

## Sites and related companies

- Authorised representative: [CMC Medical Devices & Drugs SL](https://devicerts.com/representatives/cmc-medical-devices-drugs-sl-es-ar-000000293) (Spain)

## Devices

The first 11 of 11, in the order of the canonical page, which lists them all.

- [WHILL (WHILL Model C2)](https://devicerts.com/devices/whill-whill-model-c2-iti) · ref K261175 · Class II · 510(k) · status: Active · decision 2026-06-12
- [WHILL Model R 4-wheel](https://devicerts.com/devices/whill-model-r-4-wheel-32-21014-1-03-2025-0) · ref 32-21014-1-03-2025-02-28 · Class I · EUDAMED · status: Active
- [WHILL, Inc. Model C2](https://devicerts.com/devices/whill-inc-32-00022-j-02-2024-0-a47bedc5) · Class II · GUDID · status: Active · open recall
- [WHILL, Inc. Model C2](https://devicerts.com/devices/whill-inc-32-00022-j-02-2024-0) · Class II · GUDID · status: Active · open recall
- [WHILL Model M](https://devicerts.com/devices/whill-model-m) · Class II · GUDID · status: Withdrawn
- [WHILL Model C Lite](https://devicerts.com/devices/whill-model-c-lite-32-15018-1-01-2026-0) · ref 32-15018-1-01-2026-03-06 · Class I · EUDAMED · status: Active
- [WHILL Model F](https://devicerts.com/devices/whill-model-c2-whill-model-f-whill-model-ff-whill-model-r-3-32-14016-1-04-2024-0) · ref 32-14016-1-04-2024-02-15 · Class I · EUDAMED, GUDID · status: Active
- [WHILL Model M](https://devicerts.com/devices/whill-model-m-iti) · ref K153543 · Class II · 510(k) · status: Active · decision 2016-02-12
- [WHILL Model R 3-wheel](https://devicerts.com/devices/whill-model-r-32-21014-1-03-2025-0) · ref 32-21014-1-03-2025-02-28 · Class I · EUDAMED · status: Active
- [WHILL Autonomous Model B](https://devicerts.com/devices/whill-autonomous-model-b-32-18010-0-01-2024-0) · ref 32-18010-0-01-2024-07-15 · Class I · EUDAMED · status: Active
- [WHILL Model C2](https://devicerts.com/devices/whill-model-c2-whill-model-f-whill-model-ff-whill-model-r-3-32-00022-j-02-2024-0-f605d6d8) · ref 32-00022-J-02-2024-02-15 · Class I · EUDAMED · status: Active · open recall

## FDA recalls (matched by name, newest first)

- Z-1826-2026 · Class I · Ongoing · initiated 2025-12-29 · product code ITI: Cyber vulnerability of BLE communication was found by CISA VDP program.
- Z-1827-2026 · Class I · Ongoing · initiated 2025-12-29 · product code ITI: Cyber vulnerability of BLE communication was found by CISA VDP program.

## Source and citation

- Cite as: Whill, Inc. deviCERTS medical device catalogue. https://devicerts.com/manufacturers/whill-inc (data as of 2026-11-15).
- Data sources: [EUDAMED](https://ec.europa.eu/tools/eudamed), [FDA GUDID](https://accessgudid.nlm.nih.gov/), [FDA 510(k)](https://open.fda.gov/apis/device/510k/), [FDA registration and listing](https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfrl/rl.cfm), [FDA recalls](https://open.fda.gov/apis/device/recall/)
- EUDAMED record synced: 2026-11-07
- FDA recall data as of: 2026-11-01
- Data as of: 2026-11-15
- JSON: <https://devicerts.com/manufacturers/whill-inc.json>
- Licence: [CC BY 4.0](https://creativecommons.org/licenses/by/4.0/). The deviCERTS layout and text are licensed under CC BY 4.0. Registry data remain under their source terms: U.S. FDA data (openFDA, AccessGUDID) are U.S. public domain; EUDAMED data are subject to the European Commission reuse terms.
- Attribution: DevicErts, https://devicerts.com/manufacturers/whill-inc
- Compiled by deviCERTS (devicerts.com) from public medical device registries (EUDAMED, European Commission; U.S. FDA via openFDA; AccessGUDID, U.S. National Library of Medicine). deviCERTS is not an official register and gives no regulatory advice: the record in the registry itself prevails.