John Pazienza

FDA Filings

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

FDA Registration(s)
Registration Number3003775186
FEI Number3003775186
NameJohn Pazienza
Owner & OperatorOrbusNeich Medical Company Limited (a company incorporated i
Contact AddressUnit 303 & 305, 3F, Building 20E Hong Kong Science Park
Sha Tin, N.T. HK-NA -- HK
US Agent
Registration Status1
Initial ImporterN
Registration Expiration2020-04-25
Registration Address5363 NW 35th Ave
Fort Lauderdale, FL 33309 US
Establishment TypeManufacture Medical Device

FDA Filings

Device
Company
DeviceDate
John Pazienza [OrbusNeich Medical Company Limited (a company incorporated i]
Teleport Microcatheter2019-03-18
John Pazienza [OrbusNeich Medical Company Limited (a company incorporated i]
Jade PTA2018-03-02
John Pazienza [OrbusNeich Medical Company Limited (a company incorporated i]
Sapphire II Pro2018-03-02
John Pazienza [OrbusNeich Medical Company Limited (a company incorporated i]
Sapphire II Pro Coronary Dilatation Catheter2017-08-08
John Pazienza [OrbusNeich Medical Company Limited (a company incorporated i]
Sapphire NC Plus Coronary Dilatation Catheter2017-08-08
John Pazienza [OrbusNeich Medical Company Limited (a company incorporated i]
Sapphire NC PTCA2011-09-08
John Pazienza [OrbusNeich Medical Company Limited (a company incorporated i]
Sapphire PTCA2011-09-08

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