Goldeneye Permanent System G M B H

FDA Filings

This page includes the latest FDA filings for Goldeneye Permanent System G M B H. Currently, you will find the latest 100 filings for Premarket Notifications, Premarket Applications, De Novo Applications, and GUDID registrations.

FDA Registration(s)
Registration Number3010975617
FEI Number3010975617
NameGOLDENEYE PERMANENT SYSTEM GMBH
Owner & OperatorGoldeneye Permanent System GmbH
Contact AddressMittelwegring 31 D-76751
Jockgrim DE-NOTA 76751 DE
Official Correspondent
  • Oliver Pelgen
  • 49-727-198999-10
US Agent
Registration Status1
Initial ImporterN
Registration Expiration2020-04-25
Registration AddressMittelwegring 31 D-76751
Jockgrim, 76751 DE
Establishment TypeManufacture Medical Device

FDA Filings

Device
Company
DeviceDate
Goldeneye Permanent System GmbH, Hanaim International LLC, Goldeneye Permanent System Gmbh
Otc Medication2020-02-28
GOLDENEYE PERMANENT SYSTEM GMBH
bdr Diamond Stick2020-02-06
Goldeneye Permanent System GmbH
Re-charge PH2020-02-01
GOLDENEYE PERMANENT SYSTEM GMBH
DetoxTouch2018-04-06
GOLDENEYE PERMANENT SYSTEM GMBH
DermaLift2018-04-06
GOLDENEYE PERMANENT SYSTEM GMBH
DermAbrasion2018-04-06
GOLDENEYE PERMANENT SYSTEM GMBH
Compact2018-04-06

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