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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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4 records meeting your search criteria returned- Product Code: FFO Patient Problem: No Clinical Signs, Symptoms or Conditions Report Date From: 01/1/2019
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ManufacturerBrand NameDate Report Received
INTEGRA LIFESCIENCES CORPORATION OH/USA STANDARD WISHBONE ASSEMBLY 04/19/2023
INTEGRA LIFESCIENCES CORPORATION OH/USA LAPO-CLAMP II 09/21/2022
AESCULAP AG BALFOUR ABDOMINAL RETRACTOR 200X235MM 03/15/2022
AESCULAP AG GOSSET ABDOMINAL RETRACTOR MED 55MM 09/10/2020
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