STOKO DESIGN INC.

FDA Device Registration & Listing · Vancouver British Columbia, CA · Registration 3017610538

Public Record Device Listing Expiry Year: 2026 This page presents structured fields from public FDA datasets.

Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source
FDA Device Registration & Listing
Record Type
Device registration/listing
Registration Number
3017610538
FEI Number
3017610538
Entity Name
STOKO DESIGN INC.
City/State/Country
Vancouver British Columbia, CA
Establishment Address
1535 Venables Street, Vancouver British Columbia V5L 2G8, CA
Establishment Type(s)
Manufacture Medical Device,Complaint File Establishment per 21 CFR 820.198
Owner / Operator
Stoko Design Inc. (Owner Number: 10077940)
Owner / Operator Contact Address
1535 Venables Street, Vancouver, CA-BC V5L 2G8, CA
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

Supportive Short

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
IPW Orthosis, Sacroiliac, Soft Physical Medicine Class 1 890.3490 2023-06-06

Official Correspondent

No official correspondent registered.

US Agent Details

Scott Bednar Business: QA/RA CONSULTING GROUP, INC. Email: sbednar@qaraconsultinggroup.com Phone: (412) 4188066

Related Public Records

Same Entity

Stoko Design Inc.
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 3017610538. Last updated year: 2026. Please use registration number 3017610538 when referencing this establishment in official correspondence.
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