Bob Patane

FDA Filings

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

FDA Registration(s)
Registration Number3011014178
FEI Number3011014178
NameBob Patane
Owner & OperatorKessel medintim GmbH
Contact AddressKelsterbacher Str. 28
Morfelden-Walldorf DE-HE Hessen 64546 DE
Official Correspondent
  • Martin Kessel
  • 49-6105-203720-x
US Agent
Registration Status1
Initial ImporterN
Registration Expiration2020-04-25
Registration Address1640 ROANOKE BLVD
Salem, VA 24153 US
Establishment TypeManufacture Medical Device

FDA Filings

Device
Company
DeviceDate
Bob Patane [Kessel medintim GmbH]
Vagiwell Dilators Set Small2019-11-27
Bob Patane [Kessel medintim GmbH]
Vagiwell Dilators Set Premium2019-11-27
Bob Patane [Kessel medintim GmbH]
Vagiwell Dilators Set Large2019-11-27
Bob Patane [Kessel medintim GmbH]
Rehabi Penile Vacuum Trainer2015-10-19
Bob Patane [Kessel medintim GmbH]
Manual Erection System2015-10-19
Bob Patane [Kessel medintim GmbH]
Active3 Erection System2015-10-19
Bob Patane [Kessel medintim GmbH]
Active Loop Ring2015-10-19
Bob Patane [Kessel medintim GmbH]
Active Erection System2015-10-19
Bob Patane [Kessel medintim GmbH]
Active ED System2015-10-19
Bob Patane [Kessel medintim GmbH]
Caya contoured diaphragm2015-03-03

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