• Decrease font size
  • Return font size to normal
  • Increase font size
U.S. Department of Health and Human Services

510(k) Premarket Notification

  • Print
  • Share
  • E-mail
81 to 90 of 500 Results *
Decision Date To: 07/22/2019
Results per Page
New Search  
Export all 500 Records to ExcelExport to Excel | Download Files | More About 510(k)
Device Name
Sort by Device Name [A-Z]
Sort by Device Name [Z-A]
Sort by Applicant [A-Z]
Sort by Applicant [Z-A]
Sort by 510(k) Number [0-9]
Sort by 510(k) Number [9-0]
Sort by Decision Date [0-9]
Sort by Decision Date [9-0]
hs fiber Riverpoint Medical, LLC K202242 09/10/2020
straight t clear dental aligner Straight T, Inc. K201450 09/10/2020
x-pac expandable lumbar cage system Expanding Innovations, Inc. K201145 09/10/2020
depuy synthes 2.4mm ti self-tapping matrixmandible screws (26-40mm) Synthes (USA) Products, LLC K201944 09/10/2020
dsm biomedical dental bone graft plus DSM Biomedical K193212 09/10/2020
navigation module of the momentum system ulrich medical USA K200845 09/10/2020
rgk daily range wheelchairs RGK Wheelchairs, Ltd. K200135 09/10/2020
rxsight contact lens RxSight, Inc. K201909 09/10/2020
subnovii advanced plasma technology Cartessa Aesthetics K201738 09/10/2020
tigereye cto-crossing catheter Avinger, Inc. K201330 09/10/2020

*   The maximium 500 devices meeting your search criteria returned. Please narrow your search.