WHILL (WHILL Model C2)
K-Number: K261175 · 2026-06-12
Device Summary
Frequently Asked Questions
What is the WHILL (WHILL Model C2)?
WHILL (WHILL Model C2) is a medical device that received FDA 510(k) clearance on 2026-06-12. The listed applicant is Whill, Inc.. The 510(k) number is K261175.
When did WHILL (WHILL Model C2) receive FDA 510(k) clearance?
WHILL (WHILL Model C2) received FDA 510(k) clearance on 2026-06-12, under 510(k) number K261175.
Who is the listed applicant for WHILL (WHILL Model C2)?
The FDA 510(k) record lists Whill, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for WHILL (WHILL Model C2)?
The FDA product code for WHILL (WHILL Model C2) is ITI.
Other records listing Whill, Inc. as applicant
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
Related Devices (Code: ITI)
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
Official Source
View on FDA Database →Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.