MULING CITY LONG SEN WOOD PRODUCTS LTD.

FDA Device Registration & Listing · Mudanjiang Heilongjiang, CN · Registration 3015525259

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
3015525259
FEI Number
3015525259
Entity Name
MULING CITY LONG SEN WOOD PRODUCTS LTD.
City/State/Country
Mudanjiang Heilongjiang, CN
Establishment Address
Hebeiwei, Muling Forest Office, Muling City, Mudanjiang Heilongjiang 157513, CN
Establishment Type(s)
Manufacture Medical Device for Another Party (Contract Manufacturer),Export Device to the United States But Perform No Other Operation on Device
Owner / Operator
Muling City Long Sen Wood Products Ltd. (Owner Number: 10060653)
Owner / Operator Contact Address
Hebeiwei, Muling Forest Office, Muling City, Mudanjiang, CN-HL 157513, CN
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

UTENSIL, EATING APPLICATOR, ABSORBENT TIPPED, NON-STERILE SPOON, OPHTHALMIC APPLICATOR, ABSORBENT TIPPED, STERILE

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
ILC Utensil, Eating Physical Medicine Class 1 890.5050 2019-09-24
KXF Applicator, Absorbent Tipped, Non-Sterile General Hospital Class 1 880.6025 2019-09-24
HNB Spoon, Ophthalmic Ophthalmic Class 1 886.4350 2019-09-25
KXG Applicator, Absorbent Tipped, Sterile General Hospital Class 1 880.6025 2019-09-24

Official Correspondent

Daisy Du

US Agent Details

Leeyeo Kee Business: Regrek LLC Email: regrek.cs@hotmail.com Phone: (302) 6089028

Related Public Records

Same Entity

Muling City Long Sen Wood Products Ltd.
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 3015525259. Last updated year: 2026. Please use registration number 3015525259 when referencing this establishment in official correspondence.
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