Landanger S A

FDA Filings

This page includes the latest FDA filings for Landanger S A. Currently, you will find the latest 100 filings for Premarket Notifications, Premarket Applications, De Novo Applications, and GUDID registrations.

FDA Registration(s)
Registration Number3005182241
FEI Number3005182241
NameMICHAEL S CRAWFORD
Owner & OperatorLANDANGER S.A.
Contact AddressZ.I La Vendue CS 52152
CHAUMONT CEDEX 9 FR-52 Haute-Marne 52906 FR
Official Correspondent
  • Alain GUILLAUMOT
  • 33-3-25021010-x
US Agent
Registration Status1
Initial ImporterN
Registration Expiration2020-04-25
Registration Address356 Merry Oaks Drive
Sycamore, IL 60178 US
Establishment Type
  • Manufacture Medical Device
  • Repack or Relabel Medical Device



FDA Filings

Device
Company
DeviceDate
MICHAEL S CRAWFORD [LANDANGER S.A.]
TRAY, SURGICAL2019-05-29
MICHAEL S CRAWFORD [LANDANGER S.A.]
CANNULA, SURGICAL, GENERAL & PLASTIC SURGERY2019-05-29
MICHAEL S CRAWFORD [LANDANGER S.A.]
LANDANGER2014-06-23
MICHAEL S CRAWFORD [LANDANGER S.A.]
DELACROIX-CHEVALIER2014-06-23
MICHAEL S CRAWFORD [LANDANGER S.A.]
LANDANGER2014-06-02
MICHAEL S CRAWFORD [LANDANGER S.A.]
DELACROIX-CHEVALIER2014-06-02
MICHAEL S CRAWFORD [LANDANGER S.A.]
LANDANGER2014-06-02
MICHAEL S CRAWFORD [LANDANGER S.A.]
DELACROIX-CHEVALIER2014-06-02
MICHAEL S CRAWFORD [LANDANGER S.A.]
LANDANGER1995-03-27
MICHAEL S CRAWFORD [LANDANGER S.A.]
DELACROIX-CHEVALIER1995-03-27
MICHAEL S CRAWFORD [LANDANGER S.A.]
DELACROIX CHEVALIER1995-03-27

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