FDA Device Intelligence
Home › Anika Therapeutics, Inc. › Hyalomatrix

Hyalomatrix

Anika Therapeutics, Inc. · Model 6000232 · UDI-DI 00817337000616

QSZ Prescription
1
510(k) clearances
79
Adverse events
0
Recalls
20
Facilities

Description

Hyalomatrix 2.5 cm x 2.5 cm

Query this across every FDA database — by API.

Linked GUDID · 510(k)/PMA · MAUDE · recalls · establishments. Free tier, no card required.

Get your free API keyRead the docs
Data compiled from public U.S. FDA sources (GUDID, 510(k)/PMA, MAUDE, recalls, establishment registration). Adverse-event reports are unverified and do not establish causation. Informational only — not medical, clinical, or regulatory advice.