Flextronics International Kft

FDA Device Registration & Listing · Budapest, HU · Registration 3008886285

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
3008886285
FEI Number
3008886285
Entity Name
Flextronics International Kft
City/State/Country
Budapest, HU
Establishment Address
Hangar utca 5-37, Budapest 1183, HU
Establishment Type(s)
Manufacture Medical Device for Another Party (Contract Manufacturer)
Owner / Operator
Flextronics International USA, Inc. (Owner Number: 9006592)
Owner / Operator Contact Address
12455 Research Blvd, Austin, TX 78759, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

tray, surgical, instrument - TRAYS AND RACKS.; VARIOUS TYPES OF CASES 10 Tray, Sugical instrument, Matrixrib Compact, MiniModule, Vario Case, Vario Tray, Zip Fix

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
FSM Tray, Surgical, Instrument General, Plastic Surgery Class 1 878.4800 2015-07-02

Official Correspondent

Chad Ashton

US Agent Details

Chad Ashton Business: FLEXTRONICS INTERNATIONAL USA, INC. Email: chad.ashton@flex.com Phone: (901) 8712423

Related Public Records

Same Entity

Flextronics International USA, Inc.
View consolidated registration, premarket clearance, and recall records for this applicant.
View Entity Profile →

Other Registrations for Same Entity

Registration Number Establishment Name Location
3003027964 Flex Precision Plastics Solutions (Switzerland) AG Hagglingen Aargau, CH
3006126537 FLEXTRONICS INTERNATIONAL GMBH ALTHOFEN Karnten, AT
3021010223 Flex Precision Plastics Solutions AG Kussnacht Schwyz, CH
3022473387 Flextronics Medical Molding (Shenzhen) Co., Ltd Shenzhen Guangdong, CN
3011536730 Flextronics International USA Buffalo Grove, IL, US

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 3008886285. Last updated year: 2026. Please use registration number 3008886285 when referencing this establishment in official correspondence.
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