Eisenhut Instrumente G M B H

FDA Filings

This page includes the latest FDA filings for Eisenhut Instrumente 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 Number8043507
FEI Number3000041196
NameEISENHUT INSTRUMENTE GMBH
Owner & OperatorEISENHUT INSTRUMENTE GMBH
Contact AddressSCHILDECKSTR. 28-30 --
FRITTLINGEN DE-BW Baden-Wurttemberg D-78665 DE
US Agent
Registration Status1
Initial ImporterN
Registration Expiration2020-04-25
Registration AddressSCHILDECKSTR. 28-30
FRITTLINGEN Baden-Wurttemberg, D-78665 DE
Establishment TypeRepack or Relabel Medical Device



FDA Filings

Device
Company
DeviceDate
EISENHUT INSTRUMENTE GMBH
Micro Needles for General & Plastic Surgery, Various2011-12-09
EISENHUT INSTRUMENTE GMBH
Osteotomes, Various Designs, for General Surgical Use2011-08-09

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