Puregraft

FDA Filings

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

FDA Registration(s)
Registration Number3011277972
FEI Number3011277972
NamePUREGRAFT LLC
Owner & OperatorPuregraft
Contact Address420 Stevens Avenue Suite 220
Solana Beach CA 92075 US
Registration Status1
Initial ImporterY
Registration Expiration2020-04-25
Registration Address420 Stevens Ave Ste 220
Solana Beach, CA 92075 US
Establishment TypeDevelop Specifications But Do Not Manufacture At This Facility

FDA Filings

Device
Company
DeviceDate
PUREGRAFT LLC [Puregraft]
Vacuum Lid - Port Replacement Kit2017-08-08
PUREGRAFT LLC [Puregraft]
Vacuum Lid - O-Ring Kit2017-08-08
PUREGRAFT LLC [Puregraft]
Puregraft Vacuum Lid2017-08-08
PUREGRAFT LLC [Puregraft]
Puregraft Combined Adapter2017-08-08
PUREGRAFT LLC [Puregraft]
Puregraft Instrument Set2017-05-30
PUREGRAFT LLC [Puregraft]
Puregraft 50 System2014-12-01
PUREGRAFT LLC [Puregraft]
Puregraft 850 System2014-12-01
PUREGRAFT LLC [Puregraft]
Puregraft 250 System2014-12-01

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