• 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 
 > 
 
18 records meeting your search criteria returned- Product Code: NEW Product Problem: Device Contaminated During Manufacture or Shipping Report Date From: 01/1/2019

New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
ETHICON INC. SFX SPI PDS+ UNI VIO 6IN 3-0 S/A SH 01/08/2024
ETHICON INC. PDS II SUTURE 8-18" (45CM) 4-0 VIO 10/18/2023
ETHICON INC. PDS II SUTURE 8-18" (45CM) 4-0 VIO 10/18/2023
ETHICON INC. SFX SPI PDS+ UNI VIO 6IN 4-0 S/A RB-1 08/22/2023
ETHICON INC. PDSII VIO 8X18IN 3-0 S/A SH-1 CR 06/13/2023
ETHICON INC. PDSII VIO 18IN 4-0 S/A PS-2 PRM MP 05/30/2023
ETHICON INC. PDSII VIO 8X18IN 0 S/A CTB-1 CR 05/26/2023
ETHICON INC. PDSII VIO 60IN 0 S/A TP-1 LP 05/03/2023
MEDOS INTERNATIONAL SARL ORTHOCORD - VIOLET W NEEDLES 12/PK 03/29/2023
ETHICON INC. PDSII VIO 36IN 1 S/A CTXB 03/22/2023
-
-