WHILL, INC.
2 FDA 510(k) clearances · Recalling firm
| Record | Firm | Date |
|---|---|---|
| WHILL Model C2, with software versions before HMI: 2.22 / MC: 1.13; device is an indoor/ou recall (Z-1826-2026) | WHILL, INC. | 2026-04-24 |
| WHILL Model F, with software versions before HMI: 2.23 / MC: 1.05; the device is an indoor recall (Z-1827-2026) | WHILL, INC. | 2026-04-24 |
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Every clearance here is in the API, with alerts when new ones post.