DANDONG MINGCHENG ENVIRONMENTAL PROTECTION PRODUCTS CO., LTD.

FDA Device Registration & Listing · Dandong Liaoning, CN · Registration 3043153503

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
3043153503
FEI Number
3043153503
Entity Name
DANDONG MINGCHENG ENVIRONMENTAL PROTECTION PRODUCTS CO., LTD.
City/State/Country
Dandong Liaoning, CN
Establishment Address
No. 1 Group, Qianyang Village, Qianyang Town, Donggang City, Dandong Liaoning 118301, CN
Establishment Type(s)
Manufacture Medical Device
Owner / Operator
Dandong Mingcheng Environmental Protection Products Co., Ltd (Owner Number: 10094877)
Owner / Operator Contact Address
No. 1 Group, Qianyang Village, Qianyang Town, Donggang City, Dandong, CN-LN 118301, CN
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

250ML BOWL, 500 ML BOWL

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
LRP Tray, Surgical General, Plastic Surgery Class 1 878.4800 2025-12-31

Official Correspondent

No official correspondent registered.

US Agent Details

Jessie Yao Business: MEDRIGHT TECH INC Email: info@medright-tech.com Phone: (718) 2169957

Related Public Records

Same Entity

Dandong Mingcheng Environmental Protection Products Co., Ltd
View consolidated registration, premarket clearance, and recall records for this applicant.
View Entity Profile →

Related 510(k) Records

510(k) Number Applicant Device Name Decision Date
K881095 CooperVision, Inc. KOI(TM) INSTRUMENT TRAYS 1988-04-06

Related Recall Records

Recall ID Recalling Firm Recall Class Product Description
Z-0036-2010 Alphatec Spine, Inc. 1
ROC Lumbar bolt caddy, Part Number: 81997-01-05. Sterilization container for ROC bolts/screws. Product is used to contain spinal implants.

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3043153503. Last updated year: 2026. Please use registration number 3043153503 when referencing this establishment in official correspondence.
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