FDA Device Intelligence
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Acid, Hyaluronic, Intraarticular

FDA product code MOZ · Class 3 · Unknown

104
Registered devices
8,410
Adverse events
2
Recalls
0
510(k) clearances

Devices with this code

Supartz — PAVAN TRADING LTDSUPARTZ FX sodium hyaluronate — BIOVENTUS LLCOrthovisc — MAPLESTONE DEVELOPMENTS LIMITEDHyalgan® Sodium Hylauronate Pre-filled Syringe - 2mL — FIDIA FARMACEUTICI SPASynvisc One (Synvisc Three) — PAVAN TRADING LTDHymovis® High Molecular Weight Viscoelastic Hyaluronan, 24mg/3ml syringe — FIDIA FARMACEUTICI SPADurolane — PAVAN TRADING LTDEuflexxa — DAMBO SRLSupartz — DAMBO SRLHyalgan® Sodium Hylauronate Pre-filled Syringe - 2mL — FIDIA FARMACEUTICI SPAEuflexxa — PROPHARMA-UK LTDSYNVISC ONE — FCL HEALTH SOLUTIONS LTDOrthovisc — Anika Therapeutics, Inc.Durolane — ACRE PHARMA LIMITEDArthrex® — ARTHREX, INC.Synvisc — PHARMACEUTICAL HEALTH LIMITEDEuflexxa — FCL HEALTH SOLUTIONS LTDOrthovisc — PHARMACEUTICAL HEALTH LIMITEDEuflexxa — 9902392 Canada IncSYNVISC — FCL HEALTH SOLUTIONS LTDDUROLANE — SAIMA GLOBAL FARMA S.L.Monovisc — PAVAN TRADING LTDSupartz — EAGLE SPRINGS ENTERPRISES LLCDurolane — Arcera GmbH

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.