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 
 > 
 
30 records meeting your search criteria returned- Product Code: HAB Patient Problem: Insufficient Information Report Date From: 01/1/2019

New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
SMITH & NEPHEW, INC. DYONICS 5.5MM ELITE STONECUTTER BURR 09/05/2021
SMITH & NEPHEW, INC. DYONICS 5.5MM ELITE STONECUTTER BURR 09/05/2021
SMITH & NEPHEW, INC. MOTOR DRIVE UNIT HAND CNTRL PWRMX EL 06/04/2021
SMITH & NEPHEW, INC. MOTOR DRIVE UNIT HAND CNTRL PWRMX EL 03/15/2021
AESCULAP AG ACCULAN LID 03/10/2021
SMITH & NEPHEW, INC. MOTOR DRIVE UNIT HAND CNTRL PWRMX EL 03/09/2021
ZIMMER SURGICAL SA UNIVERSAL MODULAR ELECTRIC/BATTERY SINGL 03/02/2021
SMITH & NEPHEW, INC. MOTOR DRIVE UNIT HAND CNTRL PWRMX EL 01/12/2021
CONMED CORPORATION POWERPRO TRINKLE/AO ATTACHMENT 01/11/2021
SMITH & NEPHEW, INC. SVC REPL MDU HAND CNTRL PWRMX 12/07/2020
-
-