Suturex Renodex

FDA Filings

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

FDA Registration(s)
Registration Number3003192334
FEI Number3003192334
NameSUTUREX & RENODEX S.A.
Owner & OperatorSUTUREX & RENODEX
Contact AddressZONE DE VIALARD CARSAC --
SARLAT LA CANEDA FR-24 Dordogne 24200 FR
Official Correspondent
  • Oriane - MOREAU
  • 33-5-53313484-x
US Agent
Importing Logistics Registration
ImporterS. JACKSON INC.
Address15 ROTH STREET
Alexandria, VA 22314 UNITED STATES
Importer TypeSUTURES MANUFACTURER
Registration Status1
Initial ImporterN
Registration Expiration2020-04-25
Registration AddressZONE DE VIALARD CARSAC
SARLAT LA CANEDA Dordogne, 24200 FR
Establishment TypeManufacture Medical Device



FDA Filings

Device
Company
DeviceDate
SUTUREX & RENODEX S.A. [SUTUREX & RENODEX]
XFLEX2005-06-15
SUTUREX & RENODEX S.A. [SUTUREX & RENODEX]
ENOVA2005-06-15
SUTUREX & RENODEX S.A. [SUTUREX & RENODEX]
420PLUS2005-06-15

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