Guidewire Technologies Inc

FDA Filings

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

FDA Registration(s)
Registration Number1221806
FEI Number1221806
NameGUIDEWIRE TECHNOLOGIES, INC.
Owner & OperatorGUIDEWIRE TECHNOLOGIES, INC.
Contact Address26 KEEWAYDIN DR. --
SALEM NH 03079 US
Official Correspondent
  • DOUGLAS J CURTIS
  • x-603-8944399-x
Registration Status1
Initial ImporterN
Registration Expiration2020-04-25
Registration Address26 KEEWAYDIN DR.
SALEM, NH 03079 US
Establishment TypeManufacture Medical Device

FDA Filings

Device
Company
DeviceDate
GUIDEWIRE TECHNOLOGIES, INC.
PTFE Coated Guidewire2007-12-10
GUIDEWIRE TECHNOLOGIES, INC.
Uncoated Guidewire2007-12-10
GUIDEWIRE TECHNOLOGIES, INC.
GUIDEWIRE1992-08-06
GUIDEWIRE TECHNOLOGIES, INC.
TEFLON COATED GUIDEWIRE1990-07-31
GUIDEWIRE TECHNOLOGIES, INC.
MOVABLE CORE GUIDEWIRE1990-07-31
GUIDEWIRE TECHNOLOGIES, INC.
GUIDEWIRE1989-09-12

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