Flextronics Medical Molding (Shenzhen) Co., Ltd

FDA Device Registration & Listing · Shenzhen Guangdong, CN · Registration 3022473387

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
3022473387
FEI Number
3022473387
Entity Name
Flextronics Medical Molding (Shenzhen) Co., Ltd
City/State/Country
Shenzhen Guangdong, CN
Establishment Address
1/F, 2/F, Building 1, 2/F, Building 2, And 1/F, Building 3 Rundongsheng Industrial Park, Longteng, Xixiang, Baoan District, Shenzhen Guangdong 518126, CN
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

11706799001 Assay Tip Elecsys, 11706802001 Assay Cup Elecsys, 05694302001 AssayTip/AssayCup tray (E2G) 06241620001, MagNA Pure Tip 1000?L 03755525001, SPU 05534941001, Cobas Omni Amplification Plate, 12102137001, Assay Tip/Cup Elecsys Modular, 03137082001, Tube-K Box of 12x9 08863504001, Assay Tip tray

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
LXG Equipment, Laboratory, General Purpose, Labeled Or Promoted For A Specific Medical Use Clinical Chemistry Class 1 862.2050 2015-10-20

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
3008886285 Flextronics International Kft Budapest, HU
3006126537 FLEXTRONICS INTERNATIONAL GMBH ALTHOFEN Karnten, AT
3021010223 Flex Precision Plastics Solutions AG Kussnacht Schwyz, CH
3011536730 Flextronics International USA Buffalo Grove, IL, US

Related Recall Records

Recall ID Recalling Firm Recall Class Product Description
Z-0002-2008 Beckman Coulter Inc 1
FP1000 Cell Preparation System Software versions 1.1 & 1.2, Part Number 624922, for in vitro diagnostic use.
Z-0023-2013 Biomerieux Inc 1
PREVI Isola System, Catalog numbers 29500 and 29500R, bioMerieux, Inc., Durham, NC. Intended to perform the inoculation and streaking of Prepoured Media (PPM) with liquid microbiological samples.

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3022473387. Last updated year: 2026. Please use registration number 3022473387 when referencing this establishment in official correspondence.
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