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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: HRM Product Problem: Device Dislodged or Dislocated Report Date From: 01/1/2007
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ManufacturerBrand NameDate Report Received
CARL ZEISS MEDITEC AG (OBERKOCHEN) OPMI LUMERA T 11/11/2020
CARL ZEISS MEDITEC AG (OBERKOCHEN) OPMI LUMERA I 02/28/2020
ENDURE MEDICAL, INC. LUXOR OPHTHALMIC MICROSCOPES 03/12/2019
CARL ZEISS MEDITEC AG (OBERKOCHEN) OPMI LUMERA I 06/07/2018
ALCON RESEARCH, LTD. - IRVINE TECHNOLOGY LUXOR OPHTHALMIC MICROSCOPES 06/12/2015
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