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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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5 records meeting your search criteria returned- Product Code: KMW Product Problem: Improper or Incorrect Procedure or Method Report Date From: 01/1/2007
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ManufacturerBrand NameDate Report Received
W&H DENTALWERK BUERMOOS GMBH S-12 04/16/2019
NAKANISHI INC. NSK 03/22/2018
W&H DENTALWERK BUERMOOS GMBH RIGHT ANGLED SCREWDRIVER 10/31/2017
NAKANISHI INC. NSK SGA-E2G 05/22/2014
NAKANISHI INC. NSK 05/09/2014
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