# Whill, Inc.

- Location (FDA's records): Shinagawa-Ku, JP
- FDA decisions: 5 (2016–2026): 5 510(k) clearances
- Product codes: ITI (4), INI (1)
- 510(k) review time since 2016: median 63 days, against 111 for FDA's reviews in the same codes and years (4 of 5 faster)
- Predicates its devices cite: 5 (3 its own); citations of its devices by later devices: 4 (3 its own)
- Recalls linked to its devices: 2 (2 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms whose devices it cites most
- Permobil AB: 1 (https://510kreport.com/company/permobil)
- Zhejiang Innuovo Rehabilitation Devices Co.,Ltd: 1 (https://510kreport.com/company/zhejiang-innuovo-rehabilitation-devices)

## Firms that cite its devices most
- Shanghai Bangbang Robotics Co., Ltd.: 1 (https://510kreport.com/company/shanghai-bangbang-robotics)

## Its most-cited devices
- K213383: WHILL Model C2 (2021), cited by 3
- K153543: WHILL Model M (2016), cited by 1

## Recent decisions
- K261175: WHILL (WHILL Model C2) (Jun 12, 2026)
- K242760: WHILL Model R (Jan 6, 2025)
- K221438: WHILL Model F (Jun 7, 2022)
- K213383: WHILL Model C2 (Nov 9, 2021)
- K153543: WHILL Model M (Feb 12, 2016)

Source page: https://510kreport.com/company/whill