• 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 
 > 
 
16 records meeting your search criteria returned- Product Code: QPQ Patient Problem: No Clinical Signs, Symptoms or Conditions Report Date From: 01/1/2009
New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
ORTHOSPACE LTD. UNKNOWN_ORTHOSPACE_PRODUCT 08/02/2023
ORTHOSPACE LTD. INSPACE IMPLANT - LARGE 06/29/2023
ORTHOSPACE LTD. INSPACE IMPLANT - MEDIUM 03/22/2023
STRYKER ENDOSCOPY-SAN JOSE INSPACE US MEDIUM 03/22/2023
ORTHOSPACE LTD. UNKNOWN_ORTHOSPACE_PRODUCT 03/22/2023
ORTHOSPACE LTD. INSPACE? US SMALL 03/22/2023
STRYKER ENDOSCOPY-SAN JOSE INSPACE US LARGE 07/25/2022
STRYKER ENDOSCOPY-SAN JOSE INSPACE US LARGE 07/19/2022
STRYKER ENDOSCOPY-SAN JOSE INSPACE US MEDIUM 06/22/2022
ORTHOSPACE LTD. INSPACE US LARGE 06/14/2022
-
-