Wisdom Medical Technologies

FDA Filings

This page includes the latest FDA filings for Wisdom Medical Technologies. Currently, you will find the latest 100 filings for Premarket Notifications, Premarket Applications, De Novo Applications, and GUDID registrations.

FDA Registration(s)
Registration Number3013532143
FEI Number3013532143
NameWisdom Medical Technologies
Owner & OperatorWisdom Medical Technologies
Contact Address7791 Aqua Circle, Suite 7G
Dalton Gardens ID 83815 US
Official Correspondent
  • Tony Jakubowski
  • x-800-9395812-x
Registration Status1
Initial ImporterN
Registration Expiration2020-04-25
Registration Address7791 Aqua Circle, Suite 7G
Dalton Gardens, ID 83815 US
Establishment Type
  • Manufacture Medical Device
  • Repack or Relabel Medical Device



FDA Filings

Device
Company
DeviceDate
Wisdom Medical Technologies
Leonardo HPD 980-14702017-05-23
Wisdom Medical Technologies
Evolve HPD 980-14702017-05-23
Wisdom Medical Technologies
EVOLVE? HPD 980-1470nm2017-05-23
Wisdom Medical Technologies
MegaBeam? Endo-ENT Probe2017-04-12
Wisdom Medical Technologies
MegaBeam? Single Use2017-04-12
Wisdom Medical Technologies
MegaBeam? Reusable2017-04-12
Wisdom Medical Technologies
ELVeS? Radial?2017-04-12
Wisdom Medical Technologies
ELVeS? Radial? Kit2017-04-12
Wisdom Medical Technologies
Ceralas? E 1470nm2017-04-12
Wisdom Medical Technologies
Twister Side-Fiber Optic Delivery System2017-04-05

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