Refine Usa L L C

FDA Filings

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

FDA Registration(s)
Registration Number3006033709
FEI Number3006033709
NameREFINE USA, LLC
Owner & OperatorREFINE USA, LLC
Contact Address340 3rd Avenue South
Jacksonville Beach FL 32250 US
Official Correspondent
  • brian smith
  • x-904-6290100-x
Registration Status1
Initial ImporterN
Registration Expiration2020-04-25
Registration Address340 3rd Avenue S
Jacksonville Beach, FL 32250 US
Establishment Type
  • Repack or Relabel Medical Device
  • Manufacture Medical Device

FDA Filings

Device
Company
DeviceDate
Refine Usa, LLC
 Rejuvapen 2023-07-28
Refine USA LLC
Rejuvapen NXT2020-04-09
REFINE USA, LLC
Rejuvapen2020-04-09
REFINE USA, LLC
Apex2018-06-14
REFINE USA, LLC
VEIN-GOGH INSTRUMENT2012-05-08

Related Finance Registrations
© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.