COLUMBUS CANVAS PRODUCTS

FDA Device Registration & Listing · Columbus, OH, US · Registration 3009410520

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
3009410520
FEI Number
3009410520
Entity Name
COLUMBUS CANVAS PRODUCTS
City/State/Country
Columbus, OH, US
Establishment Address
577 N 4th St, Columbus, OH 43215, US
Establishment Type(s)
Manufacture Medical Device
Owner / Operator
Columbus Healthcare Products (Owner Number: 10038654)
Owner / Operator Contact Address
577 North 4th Street, Columbus, OH 43215, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

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Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
KID Restraint, Wheelchair, Non-Protective Physical Medicine Class 1 890.3910 2011-10-31
FSD Binder, Abdominal General Hospital Class 1 880.5160 2011-10-31

Official Correspondent

Jan Kellogg

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Columbus Healthcare Products
View consolidated registration, premarket clearance, and recall records for this applicant.
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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3009410520. Last updated year: 2026. Please use registration number 3009410520 when referencing this establishment in official correspondence.
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