Ortho Plus S A

FDA Filings

This page includes the latest FDA filings for Ortho Plus 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 Number3000325615
FEI Number3000325615
NameNichole Leahy-Glass
Owner & OperatorORTHO PLUS SA
Contact Address28, RUE AMPERE -Z.I.-BP 28
IGNY FR-NOTA 91430 FR
US Agent
Registration Status1
Initial ImporterN
Registration Expiration2020-04-25
Registration Address2165 Earlywood Drive
Franklin, IN 46131 US
Establishment TypeManufacture Medical Device



FDA Filings

Device
Company
DeviceDate
Nichole Leahy-Glass [ORTHO PLUS SA]
Prepoplus Tooth Postiioner1998-04-13
Nichole Leahy-Glass [ORTHO PLUS SA]
EF Line1998-04-13

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