Alians Forearm
K-Number: K262649 · 2026-09-28
Device Summary
Frequently Asked Questions
What is the Alians Forearm?
Alians Forearm is a medical device that received FDA 510(k) clearance on 2026-09-28. The listed applicant is Newclip Technics. The 510(k) number is K262649.
When did Alians Forearm receive FDA 510(k) clearance?
Alians Forearm received FDA 510(k) clearance on 2026-09-28, under 510(k) number K262649.
Who is the listed applicant for Alians Forearm?
The FDA 510(k) record lists Newclip Technics as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Alians Forearm?
The FDA product code for Alians Forearm is HRS.
Related Clinical Trials
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.
Other records listing Newclip Technics 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: HRS)
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.