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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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24 records meeting your search criteria returned- Product Code: HJO Product Problem: Use of Device Problem Report Date From: 01/1/2007
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ManufacturerBrand NameDate Report Received
CARL ZEISS MEDITEC AG (JENA) IOLMASTER 700 12/21/2023
CARL ZEISS MEDITEC AG (JENA) IOLMASTER 700 12/21/2023
CARL ZEISS MEDITEC AG (JENA) IOLMASTER 700 12/21/2023
CARL ZEISS MEDITEC AG (JENA) IOLMASTER 700 12/20/2023
CARL ZEISS MEDITEC AG (JENA) IOL MASTER 500 04/15/2022
CARL ZEISS MEDITEC AG (JENA) IOLMASTER 500 08/27/2020
CARL ZEISS MEDITEC AG (JENA) IOLMASTER 500 02/03/2020
CARL ZEISS MEDITEC AG (JENA) IOLMASTER 700 12/20/2019
CARL ZEISS MEDITEC AG (JENA) IOLMASTER 700 12/04/2019
CARL ZEISS MEDITEC AG (JENA) IOLMASTER 700 09/27/2019
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