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U.S. Department of Health and Human Services

MAUDE - Manufacturer and User Facility Device Experience

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Super Search Devices@FDA
510(k) | DeNovo | Registration & Listing | Adverse Events | Recalls | PMA | HDE | Classification | Standards
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9 records meeting your search criteria returned- Product Code: MOZ Product Problem: Lack of Effect Report Date From: 01/1/2009
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ManufacturerBrand NameDate Report Received
ANIKA ORTHOVISC 05/24/2023
ANIKA ORTHOVISC 05/23/2023
ANIKA MONOVISC 05/22/2023
ANIKA ORTHOVISC 05/22/2023
BIO-TECHNOLOGY GENERAL (ISRAEL) LTD. EUFLEXXA 03/16/2023
BIO-TECHNOLOGY GENERAL (ISRAEL) LTD. EUFLEXXA 03/06/2023
ANIKA MONOVISC 03/02/2023
BIO-TECHNOLOGY GENERAL (ISRAEL) LTD. EUFLEXXA 02/24/2023
ANIKA MONOVISC 09/15/2022
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