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U.S. Department of Health and Human Services

Manufacturer and User Facility Device Experience (MAUDE)

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510(k) | DeNovo | Registration & Listing | Adverse Events | Recalls | PMA | HDE | Classification | Standards
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500 records meeting your search criteria returned. The results are incomplete - please narrow your search.

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ManufacturerBrand NameDate Report Received
ZIMMER BIOMET / SEIKAGAKU CORPORATION, T GEL-ONE CROSS-LINKED HYALURONATE KNEE IN 10/18/2022
BIOVENTUS LLC. DUROLANE INJECTION 10/05/2022
BIOVENTUS LLC. DUROLANE INJECTION 10/05/2022
BIOVENTUS LLC. HYALURONIC ACID INJECTION (SUPARTZ INJEC 09/28/2022
BIOVENTUS LLC. HYALURONIC ACID INJECTION (SUPARTZ INJEC 09/28/2022
GENZYME CORPORATION SYNVISC ONE 09/14/2022
GENZYME CORPORATION(RIDGEFIELD) SYNVISC 09/10/2022
BIO-TECHNOLOGY GENERAL (ISRAEL) LTD. EUFLEXXA 08/31/2022
UNKNOWN HYALURONIC PEN 08/29/2022
GENZYME CORPORATION(RIDGEFIELD) SYNVISC 08/10/2022
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