Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3003475336

FEI Number

3003475336

Entity Name

CASCADE DAFO, INC.

City/State/Country

FERNDALE, WA, US

Establishment Address

1360 Sunset Ave, FERNDALE, WA 98248, US

Establishment Type(s)

Manufacture Medical Device

Owner / Operator

CASCADE DAFO, INC. (Owner Number: 9060897)

Owner / Operator Contact Address

1360 SUNSET AVENUE, --, Ferndale, WA 98248, US

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

DAFO

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
IQI	Orthosis, Limb Brace	Physical Medicine	Class 1	890.3475	2004-02-02

Official Correspondent

Jacob Adie

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

CASCADE DAFO, INC.

View consolidated registration, premarket clearance, and recall records for this applicant.

View Entity Profile →

Similar Registrations

Registration Number	Establishment Name	Location
3005088750	3M POLAND MANUFACTURING SP. Z O.O	WROCLAW Dolnoslaskie, PL
3013001618	CAST21 INC.	Evanston, IL, US
2184046	OSBORN MEDICAL CORPORATION	CENTENNIAL, CO, US
3006979871	TRULIFE, LTD.	S. Yorkshire Sheffield, GB
3006137579	ALIGNMED INC.	Irvine, CA, US

Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3003475336. Last updated year: 2026. Please use registration number 3003475336 when referencing this establishment in official correspondence.