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
 

 
 < 
 3 
 4 
 5 
 6 
 7 
 8 
 9 
 10 
 11 
 12 
 > 
 
282 records meeting your search criteria returned- Product Code: JDR Product Problem: Adverse Event Without Identified Device or Use Problem Report Date From: 01/1/2009

New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
DEPUY MITEK LLC US UNK - IMPLANT 02/16/2022
SYNTHES GMBH UNK - BONE STAPLE: SPEED 01/05/2022
SMITH & NEPHEW, INC. UNKN METAL SUTURE ANCHOR 11/30/2021
SMITH & NEPHEW, INC. UNKN METAL SUTURE ANCHOR 11/30/2021
SMITH & NEPHEW, INC. UNKN PEEK SUTURE ANCHOR 11/28/2021
SMITH & NEPHEW, INC. UNKN PEEK SUTURE ANCHOR 11/28/2021
SMITH & NEPHEW, INC. UNKN NON-ABSORBABLE SUTURE AND TAPE 11/28/2021
SMITH & NEPHEW, INC. TWINFIX TI 5.0 ULTRABRAID 11/10/2021
DEPUY MITEK LLC US UNK - IMPLANT 10/27/2021
SMITH & NEPHEW, INC. MINITACTI 2.0 HS STR ANCHR 2 DRBRD NDL 10/18/2021
-
-