Vorotek

FDA Filings

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

FDA Registration(s)
Registration Number3007739031
FEI Number3007739031
NameVOROTEK
Owner & OperatorVorOtek
Contact Address23 Point Henry Road 23 Point Henry Road
Moolap AU-VIC Victoria 3224 AU
Official Correspondent
  • Shayne Cumming
  • 61-3-52485809-x
US Agent
Registration Status1
Initial ImporterN
Registration Expiration2020-04-25
Registration Address23 Point Henry Road
Moolap Victoria, 3224 AU
Establishment TypeComplaint File Establishment per 21 CFR 820.198



FDA Filings

Device
Company
DeviceDate
VOROTEK
VorOtek O Scope2015-10-13
VOROTEK
VorOtek LED HeadLight2015-10-13

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