Quick Links: Skip to main page content Skip to Search Skip to Topics Menu Skip to Common Links
  • Decrease font size
  • Return font size to normal
  • Increase font size
U.S. Department of Health and Human Services

Manufacturer and User Facility Device Experience (MAUDE)
  • Print
  • Share
  • E-mail
-
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
 

 
 < 
 1 
 2 
 3 
 4 
 
 
31 records meeting your search criteria returned- Product Code: PBI Patient Problem: Insufficient Information Report Date From: 01/1/2009

New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
ZIMMER BIOMET, INC. G7 HI-WALL ARCOMXL LNR 32MM G 06/06/2023
ZIMMER BIOMET, INC. G7 HI-WALL E1 LINER 36MM G 06/06/2023
ZIMMER BIOMET, INC. G7 FREEDOM CONST E1 LNR 36MM G 05/22/2023
ZIMMER BIOMET, INC. UNKNOWN LINER 05/16/2023
ZIMMER BIOMET, INC. UNKNOWN CUP 05/16/2023
ZIMMER BIOMET, INC. G7 NEUTRAL E1 LINER 36MM E 04/03/2023
ZIMMER BIOMET, INC. UNK FREEDOM LINER 03/20/2023
ZIMMER BIOMET, INC. G7 NEUTRAL E1 LINER 32MM F 04/05/2022
BIOMET UK LTD. UNK G7 BISPHERICAL CUP 02/01/2022
ZIMMER BIOMET, INC. G7 STR MONOBLOCK SHELL INSRTR 09/07/2021
-
-