Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3007341789

FEI Number

3007341789

Entity Name

SPIDERTECH INC.

City/State/Country

Toronto Ontario, CA

Establishment Address

115 Ridgetop Road, Toronto Ontario M1P 4W9, CA

Establishment Type(s)

Export Device to the United States But Perform No Other Operation on Device,Manufacture Medical Device

Owner / Operator

SPIDERTECH INC. (Owner Number: 10027702)

Owner / Operator Contact Address

115 Ridgetop Rd, Scarborough, CA-ON M1P 4W9, CA

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

Spidertech

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
FQM	Bandage, Elastic	General Hospital	Class 1	880.5075	2008-11-25

Official Correspondent

Ivie Cho

US Agent Details

FDAIMPORTS.COM LLC Email: registration@fdaimports.com Phone: (410) 2202800

Related Public Records

Same Entity

SPIDERTECH 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 3007341789. Last updated year: 2026. Please use registration number 3007341789 when referencing this establishment in official correspondence.