Lichtenheldt G M B H

FDA Filings

This page includes the latest FDA filings for Lichtenheldt 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 Number3002853327
FEI Number3002853327
NameLICHTENHELDT GMBH
Owner & OperatorLichtenheldt GmbH
Contact AddressIndustriestr. 7 - 9
Wahlstedt DE-SH Schleswig-Holstein 23812 DE
Official Correspondent
  • Florentine Grunwald
  • 049-455-49070-310
US Agent
Registration Status1
Initial ImporterN
Registration Expiration2020-04-25
Registration AddressIndustriestr. 7 - 9
Wahlstedt Schleswig-Holstein, 23812 DE
Establishment TypeManufacture Medical Device for Another Party (Contract Manufacturer)



FDA Filings

Device
Company
DeviceDate
Chiesi USA, Inc., Eurofins BioPharma Product Testing Hamburg GmbH, Amryt GmbH, CIP Chemisches Institut Pforzheim GmbH, BioChem Labor für biologische und chemische Analytik GmbH, Nuvisan GmbH, Lichtenheldt GmbH, Synergy Health Radeberg GmbH, Pharma Packaging Soluti
Prescription Medication2024-05-22
Amryt Pharmaceuticals DAC, Eurofins BioPharma Product Testing Hamburg GmbH, Amryt GmbH, CIP Chemisches Institut Pforzheim GmbH, BioChem Labor für biologische und chemische Analytik GmbH, Nuvisan GmbH, Lichtenheldt GmbH, Synergy Health Radeberg GmbH, Pharma Packagi
Prescription Medication2024-02-24
LICHTENHELDT GMBH
MagNa Pure 96 System Fluid2015-08-03

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