DANYANG CHANXIN GLASSES CASES FACTORY

FDA Device Registration & Listing · Danyang Jiangsu, CN · Registration 3013433228

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
3013433228
FEI Number
3013433228
Entity Name
DANYANG CHANXIN GLASSES CASES FACTORY
City/State/Country
Danyang Jiangsu, CN
Establishment Address
Huadian Innovation Park, Dangui Road, Development Zone,, Danyang Jiangsu 212300, CN
Establishment Type(s)
Export Device to the United States But Perform No Other Operation on Device,Manufacture Medical Device
Owner / Operator
DANYANG CHANXIN GLASSES CASES FACTORY (Owner Number: 10053069)
Owner / Operator Contact Address
Huadian Innovation Park, Dangui Road, Development Zone,, Danyang, CN-JS 212300, CN
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
K160005
PMA Number
N/A

All Registered Proprietary Names

M-BTB

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
LRX Case, Contact Lens Ophthalmic Class 2 886.5928 2016-10-28

Official Correspondent

Lemon Chen

US Agent Details

Xiang Yu Business: MZT CONSULTING INC. Email: service@mztmedtech.com Phone: (267) 3982762

Related Public Records

Same Entity

DANYANG CHANXIN GLASSES CASES FACTORY
View consolidated registration, premarket clearance, and recall records for this applicant.
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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3013433228. Last updated year: 2026. Please use registration number 3013433228 when referencing this establishment in official correspondence.
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