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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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444 records meeting your search criteria returned- Product Code: HSX Product Problem: Adverse Event Without Identified Device or Use Problem Report Date From: 01/1/2009

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ManufacturerBrand NameDate Report Received
SMITH & NEPHEW, INC. JUNI COCR FB FEM SZ 3 LM RL 03/15/2023
SMITH & NEPHEW, INC. UNKNOWN JOURNEY BCS KNEE INSERT 03/03/2023
ENCORE MEDICAL L.P EMPOWR PARTIAL KNEETM, TIBIAL INSERT, SI 02/21/2023
ENCORE MEDICAL L.P. EMPOWR PARTIAL KNEE SYSTEM 02/21/2023
ENCORE MEDICAL L.P. EMPOWR KNEE SYSTEM 02/20/2023
SMITH & NEPHEW, INC. JRNY II UNI OX FEMORAL 9 LM/RL 02/14/2023
SMITH & NEPHEW, INC. UNKNOWN JOURNEY UNI KNEE FEM COMP OX 02/06/2023
SMITH & NEPHEW, INC. UNKNOWN JOURNEY UNI KNEE FEM COMP COCR 02/06/2023
SMITH & NEPHEW, INC. JOURNEY II UK OX FEM SZ 5 RM/LL 02/03/2023
MEDACTA INTERNATIONAL SA MOTO PARTIAL KNEE TIBIAL TRAY FIX CEMENT 01/25/2023
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