Viospex

FDA Filings

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

FDA Registration(s)
Registration Number3012447313
FEI Number3012447313
NameViospex
Owner & OperatorViospex
Contact Address12919 Stroh Ranch Ct. Unit G
Parker CO 80134 US
Official Correspondent
  • Jean Bouquet
  • 1-303-8419219-x
Registration Status1
Initial ImporterN
Registration Expiration2020-04-25
Registration Address12919 Stroh Ranch Ct Unit G
Parker, CO 80134 US
Establishment TypeManufacture Medical Device



FDA Filings

Device
Company
DeviceDate
Viospex
Bouquet Vaginal Speculum2016-05-18

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