• 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: OWY Patient Problem: Pain Report Date From: 01/1/2009

New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
ROTATION MEDICAL, INC. BIOINDUCTIVE IMPLANT WITH ARTHROSCOPIC D 06/17/2021
SMITH & NEPHEW, INC. BIOINDUCTIVE IMPLANT W/ARTH DEL MED 06/16/2021
SMITH & NEPHEW, INC. BIOINDUCTIVE IMPLANT W ARTHRO DEL MED 05/14/2021
SMITH & NEPHEW, INC. BIOINDUCTIVE IMPLANT W/ARTH DEL LRG 05/13/2021
SMITH & NEPHEW, INC. BIOINDUCTIVE IMPLANT W/ARTH DEL LRG 02/19/2021
SMITH & NEPHEW, INC. BIOINDUCTIVE IMPLANT W/ARTH DEL LRG 02/18/2021
SMITH & NEPHEW, INC. REGENETEN BIOINDUCTIVE IMPLANT SYSTEM 07/14/2020
SMITH & NEPHEW, INC. ARTHRO BIOINDCTIVE 1 MED 07/12/2020
ROTATION MEDICAL, INC. ARTHRO BIOINDCTIVE 1 MED 06/13/2020
ROTATION MEDICAL, INC. TBD 05/28/2019
-
-