Signet Armorlite Inc

FDA Filings

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

Signet Armorlite Inc holds import registrations or U.S. agent authorizations in conjunction with the following organizations:

FDA Registration(s)
Registration Number2022060
FEI Number2022060
NameSIGNET ARMORLITE, INC.
Owner & OperatorSIGNET ARMORLITE, INC.
Contact Address5803 Newton Drive Suite A
Carlsbad CA 92008 US
Official Correspondent
  • PRASHANT D SANTAN
  • x-760-7444000-1356
Registration Status1
Initial ImporterY
Registration Expiration2020-04-25
Registration Address5803 Newton Dr Ste A
Carlsbad, CA 92008 US
Establishment Type
  • Manufacture Medical Device
  • Develop Specifications But Do Not Manufacture At This Facility



FDA Filings

Device
Company
DeviceDate
SIGNET ARMORLITE, INC.
KODAK UNIQUE2006-10-16
SIGNET ARMORLITE, INC.
RLX PLUS2001-11-09
SIGNET ARMORLITE, INC.
EVOCLEAR2001-11-09
SIGNET ARMORLITE, INC.
CORNING SUNSENSORS2001-11-09

Related Finance Registrations
U.S. Import Records [external site]
Import IDShipmentCargo DescriptionQuantity
2018022341593Kobe,Japan -> Los Angeles, CaliforniaPLASTIC LENSES13 CTN

© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.