Ankyras
K-Number: K230006 · 2023-12-28
Device Summary
Frequently Asked Questions
What is the Ankyras?
Ankyras is a medical device that received FDA 510(k) clearance on 2023-12-28. The listed applicant is Mentice Spain S.L.. The 510(k) number is K230006.
When did Ankyras receive FDA 510(k) clearance?
Ankyras received FDA 510(k) clearance on 2023-12-28, under 510(k) number K230006.
Who is the listed applicant for Ankyras?
The FDA 510(k) record lists Mentice Spain S.L. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Ankyras?
The FDA product code for Ankyras is PZO.
Other records listing Mentice Spain S.L. 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: PZO)
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.