Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3027605507

FEI Number

3027605507

Entity Name

Shandong Moonlight Electronics Tech Co.,Ltd.

City/State/Country

Weifang Shandong, CN

Establishment Address

Huayi Bldg, northwest corner of the intersection of Xinhua Road and Lechuan Street, Economic Development Zone, Weifang Shandong 261000, CN

Establishment Type(s)

Manufacture Medical Device

Owner / Operator

Shandong Moonlight Electronics Tech Co.,Ltd. (Owner Number: 10088202)

Owner / Operator Contact Address

Huayi Bldg, northwest corner of the intersection of Xinhua Road and Lechuan Street, Economic Development Zone, Weifang, CN-SD 261000, CN

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

Electromagnetic Stimulator Device Aqua Facial Hydrogen Oxygen Bubble System Cryolipolysis machine CO2 Fractional Laser System High Intensity Focus Ultrasound (HIFU) System Therapy Lamp, Red Light Therapy

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
NGX	Stimulator, Muscle, Powered, For Muscle Conditioning	Physical Medicine	Class 2	890.5850	2025-06-27
GFE	Brush, Dermabrasion, Powered	General, Plastic Surgery	Class 1	878.4820	2023-06-09
OOK	Dermal Cooling Pack/Vacuum/Massager	General, Plastic Surgery	Class 2	878.4340	2025-06-13
NXF	Gas, Laser Generating	General, Plastic Surgery	Class 1	878.4810	2023-06-09
PZC	Ablation System, High Intensity Focus Ultrasound (Hifu), Soft Tissue	Unknown	Class N	N/A	2023-06-09
ILY	Lamp, Infrared, Therapeutic Heating	Physical Medicine	Class 2	890.5500	2024-05-30

Official Correspondent

Ray Wang

US Agent Details

Wen Xu Email: infor@believe-med.com Phone: (443) 8968583

Related Public Records

Same Entity

Shandong Moonlight Electronics Tech 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
K221200	Xbody Hungary Kft.	XBody Go USA, XBody Pro USA	2023-01-31

Similar Registrations

Registration Number	Establishment Name	Location
3015282440	MEDICAL CABLES S.L.	Malaga, ES
3015781781	WIEMSPRO S.L	Malaga, ES
3029924973	SHENZHEN SINREL TECH LTD	Shenzhen Guangdong, CN
3013889849	Expeditors International of Washington, Inc.	Salt Lake City, UT, US
3044675848	PEPPER INTERACTIVE INC	Wilmington, DE, US

Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3027605507. Last updated year: 2026. Please use registration number 3027605507 when referencing this establishment in official correspondence.