Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3004073926

FEI Number

3004073926

Entity Name

VHA Office of Advanced Manufacturing - Ft. Lawton

City/State/Country

Seattle, WA, US

Establishment Address

4585 Texas Way W, Seattle, WA 98199, US

Establishment Type(s)

Manufacture Medical Device

Owner / Operator

VHA DEAN (Owner Number: 10077803)

Owner / Operator Contact Address

810 Vermont Ave NW, Washington, DC 20420, US

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

K222639

PMA Number

N/A

All Registered Proprietary Names

VA Thumb Splint Class 1 GMP exempt VHA Radiotherapy Bolus

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
ILH	Splint, Hand, And Components	Physical Medicine	Class 1	890.3475	2025-06-06
IXI	Block, Beam-Shaping, Radiation Therapy	Radiology	Class 2	892.5710	2023-04-05

Official Correspondent

Beth Ripley

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

VHA DEAN

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

View Entity Profile →

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3004073926. Last updated year: 2026. Please use registration number 3004073926 when referencing this establishment in official correspondence.