Centervue

FDA Filings

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

FDA Registration(s)
Registration Number3008422902
FEI Number3008422902
NamePierantonio Di Prima
Owner & OperatorCenterVue
Contact Addressvia San Marco 9h
Padova IT-34 Veneto 35129 IT
Official Correspondent
  • Luca Scienza
  • 039-049-5018399-x
US Agent
Importing Logistics Registration
ImporterIcare USA, Inc
Address4700 Falls of Neuse Rd
Raleigh, NC 27609 UNITED STATES
Importer TypeParent company, acting as distributo
Registration Status1
Initial ImporterN
Registration Expiration2020-04-25
Registration Address4700 Falls of Neuse Rd
Raleigh, NC 27609 US
Establishment TypeDevelop Specifications But Do Not Manufacture At This Facility

FDA Owner/Operator Registration

FDA Filings

Device
Company
DeviceDate
Pierantonio Di Prima [CenterVue]
DRSplus2019-12-05
Pierantonio Di Prima [CenterVue]
EIDON FA2018-07-17
Pierantonio Di Prima [CenterVue]
EIDON FA2018-07-17
Pierantonio Di Prima [CenterVue]
RETIA 22018-06-01
Pierantonio Di Prima [CenterVue]
S-MAIA2016-07-14
Pierantonio Di Prima [CenterVue]
MAIA2016-07-14
Pierantonio Di Prima [CenterVue]
S-MAIA2016-07-14
Pierantonio Di Prima [CenterVue]
MAIA2016-07-14
Pierantonio Di Prima [CenterVue]
COMPASS2015-09-24
Pierantonio Di Prima [CenterVue]
COMPASS2015-09-24
Pierantonio Di Prima [CenterVue]
EIDON2014-11-14
Pierantonio Di Prima [CenterVue]
EIDON AF2014-11-14
Pierantonio Di Prima [CenterVue]
DRS2010-11-05

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