FDA Device Intelligence
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Acid, Hyaluronic, Intraarticular

FDA product code MOZ · Class 3 · Unknown

110
Registered devices
8,445
Adverse events
2
Recalls
0
510(k) clearances

Devices with this code

Synvisc One — Arcera GmbHTriLURON — FIDIA FARMACEUTICI SPAHyalgan® Sodium Hylauronate Pre-filled Syringe - 2mL — FIDIA FARMACEUTICI SPASynvisc — MAPLESTONE DEVELOPMENTS LIMITEDMonovisc — DAMBO SRLSYNVISC — FCL HEALTH SOLUTIONS LTDSynvisc — ACRE PHARMA LIMITEDHyalgan® Sodium Hylauronate Pre-filled Syringe - 2mL — FIDIA FARMACEUTICI SPAEuflexxa — ACRE PHARMA LIMITEDSynvisc — Pharmamondis GmbHSynvisc — PHARMACEUTICAL HEALTH LIMITEDSynvisc — ALLY MEDICAL SUPPLIES LTDOrthovisc — Anika Therapeutics, Inc.TriVisc™ sodium hyaluronate — Avanos Medical, Inc.SUPARTZ® sodium hyaluronate — SEIKAGAKU CORPORATIONTRILURON — FIDIA FARMACEUTICI SPAORTHOVISC — SAIMA GLOBAL FARMA S.L.Durolane — Pharmamondis GmbHEuflexxa — FERRING PHARMACEUTICALS INC.Synvisc® — GENZYME CORPORATIONOrthovisc — PROPHARMA-UK LTDDUROLANE — SAIMA GLOBAL FARMA S.L.Synvisc — UNIVERDERMHYMOVIS® ONE Professional Sample, 32mg/4ml syringe — FIDIA FARMACEUTICI SPA

Recent recalls

DateFirmReason
2017-12-11Sanofi GenzymeContamination with Methylbacterium thiocyanatum
2010-04-16Ferring Pharmaceuticals IncOut of Specification results for molecular weight or viscosity through the established expiration date.

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Sourced from public U.S. FDA data. Informational only — not medical or regulatory advice. Not affiliated with the FDA.