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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: FZP Patient Problem: Nerve Damage Report Date From: 01/1/2019
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ManufacturerBrand NameDate Report Received
TELEFLEX MEDICAL HORIZON TI SMALL 6/CART 180/BOX 11/18/2021
US SURGICAL PUERTO RICO PREMIUM SURGICLIP II 10/13/2021
US SURGICAL PUERTO RICO PREMIUM SURGICLIP II 10/04/2021
US SURGICAL PUERTO RICO PREMIUM SURGICLIP III 09/07/2021
ETHICON ENDO-SURGERY, LLC. LIGACLIP EXTRA TITANIUM CLIPS 12/12/2019
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