• 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 
 4 
 5 
 6 
 7 
 8 
 > 
 
76 records meeting your search criteria returned- Product Code: KDD Patient Problem: No Clinical Signs, Symptoms or Conditions Report Date From: 01/1/2019

New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
STRYKER ENDOSCOPY-SAN JOSE ACL DISPOSABLE PACK-SOFT TISSUE FIXATION 04/29/2024
ALLERGAN (KELLER) KELLER FUNNEL2 (5PK) 04/04/2024
KELLER KELLER FUNNEL2 (5PK) 03/28/2024
BIOSEAL, INC. BIOSEAL BONE FLAP KIT 03/25/2024
ALLERGAN (KELLER) KELLER FUNNEL2 (5PK) 03/13/2024
STRYKER CORPORATION SOFT TISSUE FIXATION DEVICE (SINGLE USE 03/12/2024
ALLERGAN (KELLER) KELLER FUNNEL2 (5PK) 02/27/2024
ALLERGAN (KELLER) UNK KELLER FUNNEL2 02/21/2024
ALLERGAN (KELLER) UNK KELLER FUNNEL2 02/21/2024
ALLERGAN (KELLER) UNK KELLER FUNNEL2 02/13/2024
-
-