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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
CFR Title 21 | Radiation-Emitting Products | X-Ray Assembler | Medsun Reports | CLIA | TPLC
 

 
 
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11 records meeting your search criteria returned- Product Code: PAO Product Problem: Detachment Of Device Component Report Date From: 01/1/2009
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ManufacturerBrand NameDate Report Received
ZIMMER BIOMET, INC. COMP RVRS SHDR GLEN BSPLT +HA 04/06/2018
ZIMMER BIOMET, INC. GLENOID BASEPLATE 03/20/2018
ZIMMER BIOMET, INC. COMP RVRS SHLDR GLNSP STD 36MM 11/13/2017
BIOMET ORTHOPEDICS COMPREHENSIVE REVERSE SHOULDER GLENOSPHE 07/20/2017
BIOMET ORTHOPEDICS COMP RVRS SHLDR GLNSP STD 36MM 05/26/2017
BIOMET ORTHOPEDICS COMPREHENSIVE REVERSE SHOULDER GLENOSPHE 02/18/2017
BIOMET ORTHOPEDICS COMPREHENSIVE REVERSE SHOULDER CENTRAL S 02/18/2017
BIOMET, INC. COMPREHENSIVE REVERSE SHOULDER SYSTEM 11/14/2016
BIOMET ORTHOPEDICS COMP RVS HMRL TI TRAY 44MM 09/14/2016
BIOMET ORTHOPEDICS COMP RVRS SHDR GLEN BSPLT +HA 07/28/2016
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