HYALOMATRIX
K-Number: K261311 · 2026-09-02
Device Summary
Frequently Asked Questions
What is the HYALOMATRIX?
HYALOMATRIX is a medical device that received FDA 510(k) clearance on 2026-09-02. The listed applicant is Anika Therapeutics, Inc.. The 510(k) number is K261311.
When did HYALOMATRIX receive FDA 510(k) clearance?
HYALOMATRIX received FDA 510(k) clearance on 2026-09-02, under 510(k) number K261311.
Who is the listed applicant for HYALOMATRIX?
The FDA 510(k) record lists Anika Therapeutics, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for HYALOMATRIX?
The FDA product code for HYALOMATRIX is QSZ.
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 Anika Therapeutics, 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: QSZ)
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.