Hgr Instrumente G M B H

FDA Filings

This page includes the latest FDA filings for Hgr 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 Number8044098
FEI Number3004028763
NameFranz Menean
Owner & OperatorHGR INSTRUMENTE GMBH
Contact AddressSattlerstrasse 35 --
TUTTLINGEN DE-BW Baden-Wurttemberg 78532 DE
US Agent
Importing Logistics Registration
ImporterKrause Surgical Instrument Corp.
Address5544 Robertwood Dr.
Saint Louis, MO 63128 UNITED STATES
Importer TypeRetailer
Registration Status1
Initial ImporterN
Registration Expiration2020-04-25
Registration Address112 CORPORATE DR
Portsmouth, NH 03801 US
Establishment TypeManufacture Medical Device for Another Party (Contract Manufacturer)



FDA Filings

Device
Company
DeviceDate
Franz Menean [HGR INSTRUMENTE GMBH]
Ball Probe medium2012-04-19
Franz Menean [HGR INSTRUMENTE GMBH]
Ball Probe large2012-04-19
Franz Menean [HGR INSTRUMENTE GMBH]
GROSSMAN FACIAL ELEV 6-3/41999-12-20

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