Ortoway L L C

FDA Filings

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

FDA Registration(s)
Registration Number3009596010
FEI Number3009596010
NameOrtoway LLC
Owner & OperatorOrtoway AB
Contact AddressSvaerdvaegen 21
Danderyd SE-NOTA SE-182 33 SE
Registration Status1
Initial ImporterN
Registration Expiration2020-04-25
Registration Address2 Walnut Grove Dr
Horsham, PA 19044 US
Establishment TypeManufacture Medical Device for Another Party (Contract Manufacturer)



FDA Filings

Device
Company
DeviceDate
Ortoway LLC [Ortoway AB]
OrtoWell Distractor2012-04-30

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