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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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6 records meeting your search criteria returned- Product Code: JDR Product Problem: Failure to Advance Report Date From: 01/1/2017
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ManufacturerBrand NameDate Report Received
DEPUY MITEK LLC US MINI QA+ #2/O OCORD V-5 06/03/2019
DEPUY MITEK LLC US MINI QA+ #2/O OCORD V-5 06/03/2019
DEPUY MITEK LLC US FASTIN 4.0MM #2 ETH *EA 04/02/2019
CONMED CORPORATION STAPLIZER HANDPIECE 03/04/2019
ZIMMER BIOMET, INC. TOGGLELOC 2.9MM W/NDLS 10/23/2018
BIO MEDICAL ENTERPRISES INC SPEEDTRIAD COMPRESSION IMPLANT KIT 18X15 11/10/2017
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