Oneortho

FDA Filings

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

FDA Registration(s)
Registration Number3016678120
FEI Number3016678120
NameONEORTHO
Owner & OperatorONEORTHO
Contact Address206 ROUTE DE VOURLE,
SAINT GENIS LAVAL FR-69 Rhone 69230 FR
Official Correspondent
  • CHRISTOPHE ALEPEE
  • 33-670-750511-x
US Agent
Registration Status1
Initial ImporterN
Registration Expiration2020-04-25
Registration Address206 ROUTE DE VOURLE,
SAINT GENIS LAVAL Rhone, 69230 FR
Establishment TypeManufacture Medical Device for Another Party (Contract Manufacturer)



FDA Filings

Device
Company
DeviceDate
ONEORTHO
Quantum Total Ankle Prosthesis2020-03-19

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