Medicor Hand Instrument Co

FDA Filings

This page includes the latest FDA filings for Medicor Hand Instrument Co. Currently, you will find the latest 100 filings for Premarket Notifications, Premarket Applications, De Novo Applications, and GUDID registrations.

FDA Registration(s)
Registration Number9680519
FEI Number3002631673
NameBeate Weiss-Krull
Owner & OperatorMEDICOR HAND INSTRUMENT CO.
Contact AddressFUREDI UT 98 --
DEBRECEN HU-NOTA H - 4032 HU
Official Correspondent
  • PETER - NAGY
  • 36-52-310696-x
US Agent
Registration Status1
Initial ImporterN
Registration Expiration2020-04-25
Registration Address1050 SW 6th Ave., Suite 1100
Portland, OR 97204 US
Establishment Type
  • Manufacture Medical Device
  • Manufacture Medical Device for Another Party (Contract Manufacturer)

FDA Filings

Device
Company
DeviceDate
Beate Weiss-Krull [MEDICOR HAND INSTRUMENT CO.]
BE4652017-02-28
Beate Weiss-Krull [MEDICOR HAND INSTRUMENT CO.]
GL19402017-02-28
Beate Weiss-Krull [MEDICOR HAND INSTRUMENT CO.]
GL19302017-02-28
Beate Weiss-Krull [MEDICOR HAND INSTRUMENT CO.]
GL19202017-02-28
Beate Weiss-Krull [MEDICOR HAND INSTRUMENT CO.]
GL19102017-02-28
Beate Weiss-Krull [MEDICOR HAND INSTRUMENT CO.]
GL19022017-02-28
Beate Weiss-Krull [MEDICOR HAND INSTRUMENT CO.]
SU61362017-02-28
Beate Weiss-Krull [MEDICOR HAND INSTRUMENT CO.]
SU61352017-02-28
Beate Weiss-Krull [MEDICOR HAND INSTRUMENT CO.]
SU61322017-02-28
Beate Weiss-Krull [MEDICOR HAND INSTRUMENT CO.]
SU61302017-02-28
Beate Weiss-Krull [MEDICOR HAND INSTRUMENT CO.]
SU61292017-02-28
Beate Weiss-Krull [MEDICOR HAND INSTRUMENT CO.]
OS9252013-03-19
Beate Weiss-Krull [MEDICOR HAND INSTRUMENT CO.]
PB-225-28,PB-503-12, PB-710-17,PB-714-17,PB-728-18,PB-728-23,PB-797-12,RF-774-01,RO-218-24,2010-03-02
Beate Weiss-Krull [MEDICOR HAND INSTRUMENT CO.]
GL32001994-02-09

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