• 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
71 to 80 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]
hair growth system Xuzhou Kernel Medical Equipment Co., Ltd. K190685 07/26/2019
halley resin system Dentsply Sirona K191427 08/26/2019
healthpnx Zebra Medical Vision Ltd. K190362 05/06/2019
hedron cervical spacers Globus Medical Inc. K191243 09/17/2019
hedron lumbar spacers Globus Medical Inc. K191391 09/18/2019
hemotrol duo low, hemotrol duo normal, hemotrol duo high Eurotrol B.V. K192842 11/15/2019
hydrofera blue ready - border Hydrofera, LLC K190268 11/06/2019
imagingring system on rails MedPhoton GmbH K191267 08/01/2019
inclusive titanium abutments compatible with: dentsply implants astra tech implant system ev Prismatik Dentalcraft, Inc. K191222 08/05/2019
infinity fixation system ConMed Corporation K191204 07/03/2019

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