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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
CFR Title 21 | Radiation-Emitting Products | X-Ray Assembler | Medsun Reports | CLIA | TPLC
 

 
 
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11 records meeting your search criteria returned- Product Code: JDG Product Problem: Malposition of Device Report Date From: 01/1/2017
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ManufacturerBrand NameDate Report Received
SMITH & NEPHEW ORTHOPAEDICS AG EP-FIT PLUS SHELL 10/18/2022
SMITH & NEPHEW, INC. UNKN TRIGEN INTERTAN INTERTROCH ANTEGR N 04/08/2022
SMITH & NEPHEW, INC. UNKN R3 SHELL 03/15/2022
DEPUY ORTHOPAEDICS INC US TRI-LOCK TI 8.8 STD OFFSET 02/20/2020
STRYKER ORTHOPAEDICS-MAHWAH UNKNOWN SECURFIT SHELL 12/11/2018
STRYKER ORTHOPAEDICS-MAHWAH UNKNOWN SHELL 12/11/2018
ZIMMER BIOMET, INC. UNKNOWN STEM 09/12/2018
STRYKER ORTHOPAEDICS-MAHWAH UNKNOWN TRIDENT CUP 02/27/2018
BIOMET ORTHOPEDICS UNKNOWN PATELLA 08/02/2017
ZIMMER, INC. UNKNOWN LINER 03/09/2017
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