Glenn Kowalski

FDA Filings

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

FDA Registration(s)
Registration Number3010078417
FEI Number3010078417
NameGlenn Kowalski
Owner & OperatorActegy Ltd.
Contact AddressReflex Cain Road
Bracknell, Berks GB-UKM United Kingdom RG12 1HL GB
Official Correspondent
  • Roseanna Penny
  • 044-1344-636940-2027
US Agent
Registration Status1
Initial ImporterN
Registration Expiration2020-04-25
Registration Address6400 Shafer Court Suite 225
Des Plaines, IL 60018 US
Establishment Type
  • Develop Specifications But Do Not Manufacture At This Facility
  • Repack or Relabel Medical Device

FDA Filings

Device
Company
DeviceDate
Glenn Kowalski [Actegy Ltd.]
Revitive Medic2016-09-07
Glenn Kowalski [Actegy Ltd.]
Revitive Advanced2016-09-07
Glenn Kowalski [Actegy Ltd.]
Revitive Medic2016-09-07
Glenn Kowalski [Actegy Ltd.]
Revitive Advanced2016-09-07
Glenn Kowalski [Actegy Ltd.]
Revitive Circulation Booster2015-03-30
Glenn Kowalski [Actegy Ltd.]
Revitive Circulation Booster2015-03-30
Glenn Kowalski [Actegy Ltd.]
Aerosure Medic2015-03-30
Glenn Kowalski [Actegy Ltd.]
Revitive Electrode Pads2014-10-13
Glenn Kowalski [Actegy Ltd.]
Revitive Medic2013-07-31
Glenn Kowalski [Actegy Ltd.]
Revitive IX2013-07-31

Similar & Related FDA Registered Companies

Related Finance Registrations
U.S. Import Records [external site]
Import IDShipmentCargo DescriptionQuantity
2020081185624Yantian,China (Mainland) -> Los Angeles, CaliforniaTIME PIECE ACCESSORY1 PCS
© 2025 FDA.report
This site is not affiliated with or endorsed by the FDA.