Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3003701178

FEI Number

3003701178

Entity Name

SIAM INTERMAGNATE CO., LTD.

City/State/Country

BANGKOK Krung Thep Maha Nakhon, TH

Establishment Address

138 ROMKLAO ROAD, KLONGSAMPRAVED, LADKRABANG, BANGKOK Krung Thep Maha Nakhon 10520, TH

Establishment Type(s)

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

Owner / Operator

SIAM INTERMAGNATE CO., LTD. (Owner Number: 9059961)

Owner / Operator Contact Address

138, ROMKLAO ROAD, KLONGSAMPRAVED,, LADKRABANG, TH-10 10520, TH

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

No proprietary names listed under this establishment.

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
FNY	Basin, Emesis	General Hospital	Class 1	880.6730	2003-12-03
KER	Container, Embedding	Pathology	Class 1	864.3010	2003-12-03
FSM	Tray, Surgical, Instrument	General, Plastic Surgery	Class 1	878.4800	2003-12-03
KYW	Container, Liquid Medication, Graduated	General Hospital	Class 1	880.6430	2003-12-03
FNP	Urinal	General Hospital	Class 1	880.6730	2007-12-10

Official Correspondent

No official correspondent registered.

US Agent Details

Jay Mansour Business: Mansour Consulting LLC Email: jay@mansourconsulting.com Phone: (678) 9088180

Related Public Records

Same Entity

SIAM INTERMAGNATE CO., LTD.

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

View Entity Profile →

Related Recall Records

Recall ID	Recalling Firm	Recall Class	Product Description
Z-0027-2016	Zimmer, Inc.	1	Zimmer Universal Locking System, Titanium 3.5mm. Zimmer Implant and Instrument Cases are reusable, non-implantable devices designed to facilitate organization, identification, storage, transportation, cleaning, and sterilization processing of reusable instruments and certain unused implantable devices.

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3003701178. Last updated year: 2026. Please use registration number 3003701178 when referencing this establishment in official correspondence.