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
 

 
 < 
 5 
 6 
 7 
 8 
 9 
 10 
 11 
 12 
 13 
 14 
 > 
 
210 records meeting your search criteria returned- Product Code: JDR Report Date From: 1/1/2021 Report Date To: 12/31/2021

New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
SMITH & NEPHEW, INC. TWINFIX TI 5.0 ULTRABRAID 07/07/2021
SMITH & NEPHEW, INC. OSTEORAPTOR 2.9 W/ 2 UB WHITE / BLUE 07/07/2021
SMITH & NEPHEW, INC. OSTEORAPTOR 2.9 W/ 2 UB WHITE / BLUE 07/07/2021
ZIMMER BIOMET, INC. UNK ALL THREAD TITANIUM ANCHOR 07/06/2021
DEPUY MITEK LLC US SUPER QA+ O/C DS CP-2 *EA 06/28/2021
DEPUY MITEK LLC US SUPER QA+ O/C DS CP-2 *EA 06/28/2021
ARTHREX, INC. SUPERMX COMPRESSION STAPLE, 18W X 18L 06/28/2021
NEXTREMITY SOLUTIONS, INC. ARCUS STAPLE SYSTEM 06/22/2021
SMITH & NEPHEW, INC. TWINFIX TI 3.5 ULTRABRAID 06/18/2021
SMITH & NEPHEW, INC. MNITAC 2.0 TI W/NDL 22-0 ULTRABRAID 06/09/2021
-
-