Medical device makerLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field. in JapanLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field.. FDA records under 2 spellings of its name, each linked to the record.
As of Nov 14, 2026, FDA's public records list WHILL with 5 510(k) clearances and 2 device recalls. The most recent is a 510(k) clearance dated Jun 12, 2026: WHILL (WHILL Model C2).
Drug approvals, 510(k) clearances, recalls and letters, 2017 to 2026 to date
A hatched bar is a year that is not over, so its count covers only part of the year.
| Jun 12, 2026 | WHILL (WHILL Model C2)K261175 · ITI | 510(k) clearances |
| Dec 29, 2025 | WHILL Model C2, with software versions before HMI: 2.22 / MC: 1.13; device is an indoor/outdoor battery-operated 2-wheel drive (rear-wheel dClass I · Cyber vulnerability of BLE communication was found by CISA VDP program. | Device recalls |
| Dec 29, 2025 | WHILL Model F, with software versions before HMI: 2.23 / MC: 1.05; the device is an indoor/outdoor, foldable battery-operated 2-wheel drive Class I · Cyber vulnerability of BLE communication was found by CISA VDP program. | Device recalls |
| Jan 6, 2025 | WHILL Model RK242760 · INI | 510(k) clearances |
| Jun 7, 2022 | WHILL Model FK221438 · ITI | 510(k) clearances |
| Nov 9, 2021 | WHILL Model C2K213383 · ITI | 510(k) clearances |
| Feb 12, 2016 | WHILL Model MK153543 · ITI | 510(k) clearances |
Spellings are joined only when they reduce to the same name, or a reviewed source names the same company. Sharing an FDA establishment number (FEI) is not enough: contract sites make products for many firms. Facts marked AI were labelled by a language model from the firm's FDA names; everything else comes from FDA or Wikidata. How this page is built
