Nupak Medical

FDA Filings

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

FDA Registration(s)
Registration Number1649669
FEI Number3001451805
NameNuPak Medical
Owner & OperatorKATENA PRODUCTS, INC.
Contact Address6 CAMPUS DRIVE SUITE 310
Parsippany NJ 07054 US
Official Correspondent
  • BRYAN E WEINMANN
  • x-973-9891600-1014
Registration Status1
Initial ImporterN
Registration Expiration2020-04-25
Registration Address11849 STARCREST DR.
SAN ANTONIO, TX 78247 US
Establishment Type
  • Manufacture Medical Device
  • Manufacture Device in the United States for Export Only
  • Manufacture Medical Device for Another Party (Contract Manufacturer)
  • Repack or Relabel Medical Device

FDA Filings

Device
Company
DeviceDate
NuPak Medical [KATENA PRODUCTS, INC.]
Rescue Cath2017-11-10
NuPak Medical [KATENA PRODUCTS, INC.]
Eagle Flex; EaglePlug; Plug 1; SuperEagle; SuperFlex2016-10-08
NuPak Medical [KATENA PRODUCTS, INC.]
EaglePlug TearFlow; Flow Controller2016-10-08
NuPak Medical [KATENA PRODUCTS, INC.]
Punctal Gauge1993-01-01
NuPak Medical [KATENA PRODUCTS, INC.]
Eagle1993-01-01

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