SHANGHAI GREELOY INDUSTRY CO., LTD

FDA Device Registration & Listing · Shanghai, CN · Registration 3010493153

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
3010493153
FEI Number
3010493153
Entity Name
SHANGHAI GREELOY INDUSTRY CO., LTD
City/State/Country
Shanghai, CN
Establishment Address
6 Building, Songhuang road 999#,, Qingpu District, Shanghai 201706, CN
Establishment Type(s)
Manufacture Medical Device for Another Party (Contract Manufacturer),Manufacture Medical Device
Owner / Operator
Shanghai Greeloy Industry Co., Ltd (Owner Number: 10050455)
Owner / Operator Contact Address
6 Building, Songhuang road 999#,, Qingpu District, Shanghai, CN-SH 201706, CN
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

DENTAL OPERATION LIGHT PORTABLE DENTAL CHAIR CURING LIGHT Medical Air Compressor Dental Chair Without Operative Unit Medical Suction Unit AMALGAM SEPARATOR

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
EAZ Light, Operating, Dental Dental Class 1 872.4630 2017-12-19
FZK Chair, Surgical, Non-Electrical General, Plastic Surgery Class 1 878.4950 2018-10-29
EEG Heat Source For Bleaching Teeth Dental Class 1 872.6475 2018-10-29
BTI Compressor, Air, Portable Anesthesiology Class 2 868.6250 2015-11-19
NRU Chair, Dental, Without Operative Unit Dental Class 1 872.6250 2015-11-19
EBR Unit, Suction Operatory Dental Class 1 872.6640 2015-11-19

Official Correspondent

Mingbao Lu

US Agent Details

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

Related Public Records

Same Entity

Shanghai Greeloy Industry 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
K900686 Medical Industries America, Inc. MAXI COMPRESSORS 1990-04-26

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3010493153. Last updated year: 2026. Please use registration number 3010493153 when referencing this establishment in official correspondence.
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