Loriann Baranauskas

FDA Filings

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

FDA Registration(s)
Registration Number3003587170
FEI Number3003587170
NameLoriann Baranauskas
Owner & OperatorNITTO DENKO CORP.
Contact Address1-1-2, SHIMOHOZUMI --
IBARAKI CITY JP-27 Osaka 5678680 JP
US Agent
Registration Status1
Initial ImporterN
Registration Expiration2020-04-25
Registration Address125 FORTUNE BLVD
Milford, MA 01757 US
Establishment TypeManufacture Medical Device



FDA Filings

Device
Company
DeviceDate
Loriann Baranauskas [NITTO DENKO CORP.]
Spidertech tape2008-12-04
Loriann Baranauskas [NITTO DENKO CORP.]
Spidertech gentle tape2008-12-04

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