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

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
 

 
 
9 records meeting your search criteria returned- Product Code: INK Patient Problem: Muscle/Tendon Damage Report Date From: 01/1/2009
New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
STRYKER MEDICAL-KALAMAZOO PRIME ZOOM STRETCHER30INLITTER 06/28/2023
STRYKER MEDICAL-KALAMAZOO ZOOM STRETCHER, PRIME X 03/14/2023
STRYKER MEDICAL-KALAMAZOO PRIME ZOOM STRETCHER, ELECTRIC 03/01/2023
STRYKER MEDICAL-KALAMAZOO ZOOM STRETCHER, PRIME X 10/24/2022
STRYKER MEDICAL-KALAMAZOO PRIME ZOOM STRETCHER30INLITTER 04/26/2022
STRYKER MEDICAL-KALAMAZOO PRIME ZOOM STRETCHER26INLITTER 08/31/2021
STRYKER MEDICAL-KALAMAZOO PRIME ZOOM STRETCHER26INLITTER 08/27/2021
Unknown Manufacturer PRIME ZOOM STRETCHER26INLITTER 07/21/2021
STRYKER MEDICAL-KALAMAZOO PRIME ZOOM STRETCHER, ELECTRIC 03/18/2021
-
-