• Decrease font size
  • Return font size to normal
  • Increase font size
U.S. Department of Health and Human Services

MAUDE - Manufacturer and User Facility Device Experience

  • 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 
 > 
 
25 records meeting your search criteria returned- Product Code: NEW Patient Problem: Purulent Discharge Report Date From: 01/1/2018
New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
ETHICON INC. SFX SPI PDS+ UNI 12IN 4-0 SA PS-2 PRM MP 11/17/2022
ETHICON INC. SFX SPI PDS+ UNI 12IN 4-0 SA PS-2 PRM MP 11/17/2022
ETHICON INC. PDS II POLYDIOXANONE SUTURE UNKNOWN PROD 11/15/2022
SURGICAL SPECIALTIES MEXICO S. DE. R.L. STRATAFIX 09/14/2022
ETHICON INC. PDS+ VIO 27IN 4-0 S/A FS-2 07/26/2022
ETHICON INC. PDS II POLYDIOXANONE SUTURE UNKNOWN PROD 07/06/2022
SURGICAL SPECIALTIES MEXICO S. DE. R.L. STRATAFIX 06/17/2022
ETHICON INC. STRATAFIX SPIRAL PDS PLUS UNKNOWN 06/09/2022
ETHICON INC. PDS PLUS VIO 8X18IN 1 S/A CTB-1 CR 04/21/2022
ETHICON INC. SFX SPI PDS+ UNI 18IN 4-0 SA PS-2 PRM MP 03/02/2022
-
-