• 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 
 
 
11 records meeting your search criteria returned- Product Code: NHB Product Problem: Patient Device Interaction Problem Report Date From: 01/1/2009
New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
ENTELLUS MEDICAL, INC. LATERA 24MM, FINAL KIT 02/26/2024
ENTELLUS MEDICAL, INC. LATERA 24MM IMPLANT 2 12/19/2023
ENTELLUS MEDICAL, INC. LATERA 24MM, FINAL KIT 12/06/2023
ENTELLUS MEDICAL, INC. LATERA 24MM, FINAL KIT 03/14/2023
ENTELLUS MEDICAL, INC. LATERA 20MM, FINAL KIT 12/13/2021
ENTELLUS MEDICAL, INC. UNKNOWN_ENTELLUSSPIROX_PRODUCT 08/09/2021
ENTELLUS MEDICAL, INC. LATERA 24MM, FINAL KIT 07/26/2021
ENTELLUS MEDICAL, INC. LATERA ABSORBABLE NASAL 2 IMPLANTS GEN 1 05/25/2021
ENTELLUS MEDICAL, INC. LATERA 24MM, FINAL KIT 12/05/2020
ENTELLUS MEDICAL, INC. LATERA ABSORBABLE NASAL 09/11/2020
-
-