Nolato Meditech

FDA Filings

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

FDA Registration(s)
Registration Number3010288227
FEI Number3010288227
NameRussell Steele
Owner & OperatorNolato MediTech
Contact AddressMedicingatan 4
H?rby SE-M Skane lan [SE-12] 24293 SE
Official Correspondent
  • Arlene Dahl
  • 46-415-19700-x
US Agent
Registration Status1
Initial ImporterN
Registration Expiration2020-04-25
Registration Address660 Vandeberg St
Baldwin, WI 54002 US
Establishment TypeManufacture Medical Device



FDA Filings

Device
Company
DeviceDate
Russell Steele [Nolato MediTech]
Vaginal Applicator2016-09-14

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