FABRICANTES DE BASCULAS TORREY SA DE CV

FDA Device Registration & Listing · MONTERREY Nuevo Leon, MX · Registration 1000557421

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
1000557421
FEI Number
1000557421
Entity Name
FABRICANTES DE BASCULAS TORREY SA DE CV
City/State/Country
MONTERREY Nuevo Leon, MX
Establishment Address
AV. LOS ANDES 605, COL. COYOACAN, MONTERREY Nuevo Leon 64510, MX
Establishment Type(s)
Manufacture Medical Device for Another Party (Contract Manufacturer)
Owner / Operator
PELSTAR LLC (Owner Number: 9914066)
Owner / Operator Contact Address
9500 West 55th Street, McCook, IL 60525, US
Initial Importer Flag
N
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
MRL Scale, Sponge, Surgical, Electrically-Powered General Hospital Class 1 880.2740 2026-02-18
FRW Scale, Patient General Hospital Class 1 880.2720 2002-08-19

Official Correspondent

Bhupendra Shah

US Agent Details

Bhupendra Shah Business: Pelstar LLC Email: bshah@homscales.com Phone: (708) 3770564

Related Public Records

Same Entity

PELSTAR LLC
View consolidated registration, premarket clearance, and recall records for this applicant.
View Entity Profile →

Other Registrations for Same Entity

Registration Number Establishment Name Location
3014926306 Soehnle Industrial Solutions GmbH Backnang Baden-Wurttemberg, DE
3010285795 Transcell Electronics Scale Co., Ltd. Nanjing Jiangsu, CN
3004018235 Momert Zrt. Dunaujvaros Fejer, HU
3005477990 Wuxi Weigher Factory Co. Ltd. Wuxi City Jiangsu, CN
3020212802 EKS Kowloon, HK

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 1000557421. Last updated year: 2026. Please use registration number 1000557421 when referencing this establishment in official correspondence.
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