Sintea Plustek L L C

FDA Filings

This page includes the latest FDA filings for Sintea Plustek 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 Number1066481
FEI Number3003428720
NameSINTEA PLUSTEK LLC
Owner & OperatorSintea Plustek, LLC
Contact Address407 Lincoln Road, Suite 10L
Miami Beach FL 33139 US
Official Correspondent
  • Guido Zorzoli
  • x-305-6736226-x
Registration Status1
Initial ImporterY
Registration Expiration2020-04-25
Registration Address407 Lincoln Road Suite 10L
Miami Beach, FL 33139 US

FDA Filings

Device
Company
DeviceDate
SINTEA PLUSTEK, LLC
PLS (POSTERIOR LUMBAR SYSTEM)2014-05-30
SINTEA PLUSTEK, LLC
SPIDER SYSTEM KOLIBRI CEMENT NEEDLE2013-04-01
SINTEA PLUSTEK, LLC
SINTEA PLUSTEK ANTERIOR CERVICAL PLATE SYSTEM2012-02-24

Related Finance Registrations
NCAGE Code7F6H7SINTEA PLUSTEK LLC
CAGE Code7F6H7SINTEA PLUSTEK LLC
S.A.M. Registration7F6H7 [79917057]SINTEA PLUSTEK LLC
© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.