Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3000099306

FEI Number

3000099306

Entity Name

UPPER CANADA SOAP & CANDLE MAKERS

City/State/Country

Mississauga Ontario, CA

Establishment Address

5875 Chedworth Way, Mississauga Ontario L5R3L9, CA

Establishment Type(s)

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

Owner / Operator

Upper Canada Soap & Candle Makers Corporation (Owner Number: 10045233)

Owner / Operator Contact Address

5875 Chedworth Way, Mississauga, CA-ON L5R3L9, CA

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

Danielle Creations All About Men Danielle Yes Studio All About Men Cedar & Sage Danielle Cedar & Sage Hot/Cold Pack Ice Pack TheraWell TheraWell Danielle Yes Studio Cedar & Sage Danielle Creations Yes Studio Danielle Cedar & Sage

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
EFS	Unit, Oral Irrigation	Dental	Class 1	872.6510	2024-12-24
LCN	Scraper, Tongue	Dental	Class 1	872.6855	2024-12-24
EHY	Tray, Impression, Preformed	Dental	Class 1	872.6880	2024-12-24
IME	Pack, Hot Or Cold, Reusable	Physical Medicine	Class 1	890.5700	2013-10-29
ISA	Massager, Therapeutic, Electric	Physical Medicine	Class 1	890.5660	2024-12-24
NXB	Dispenser, Solid Medication	Physical Medicine	Class 1	890.5050	2024-12-24
EFW	Toothbrush, Manual	Dental	Class 1	872.6855	2024-12-24
JES	Floss, Dental	Dental	Class 1	872.6390	2024-12-24

Official Correspondent

Stephen Flatt

US Agent Details

Stephen Flatt Email: mnguyen@uppercanadasoap.com Phone: (917) 5969850

Related Public Records

Same Entity

Upper Canada Soap & Candle Makers Corporation

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

View Entity Profile →

Related 510(k) Records

510(k) Number	Applicant	Device Name	Decision Date
K844318	Pro Pulse, Inc.	ORAL IRRIGATION TIP	1984-11-23
K944481	Garan Scientific, Inc.	THE HEART PROTECTOR	1995-04-10
K973236	Procter & Gamble Co.	CREST TOOTHBRUSH WITH MICROSHIELD	1998-03-11
K882164	Arthur Blank & Co., Inc.	FLOSS CARD	1988-06-10

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3006572778	IN'TECH INDUSTRIES	Ramsey, MN, US
3005607635	HI-P (XIAMEN) PRECISION PLASTIC MANUFACTURING CO.,	XIAMEN Fujian, CN
3010162782	PROVIDENCE ENTERPRISE LIMITED	Shenzhen Guangdong, CN

Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3000099306. Last updated year: 2026. Please use registration number 3000099306 when referencing this establishment in official correspondence.