OJAN BEAUTY COMPANY LIMITED

FDA Device Registration & Listing · Guangzhou Guangdong, CN · Registration 3015967269

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
3015967269
FEI Number
3015967269
Entity Name
OJAN BEAUTY COMPANY LIMITED
City/State/Country
Guangzhou Guangdong, CN
Establishment Address
Room 705 ,7 Floor, Hetai Building, NO 89 of Hetai Road, Baiyun District, Guangzhou Guangdong 510000, CN
Establishment Type(s)
Manufacture Medical Device
Owner / Operator
OJAN BEAUTY COMPANY LIMITED (Owner Number: 10062592)
Owner / Operator Contact Address
Room 705 ,7 Floor, Hetai Building, NO 89 of Hetai Road, Baiyun District, Guangzhou, CN-GD 510000, CN
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

Skin scrubber Electric In Home Facial Massager Nuderma Clinical New Spa Professional Grade Portable High Frequency D'arsonval Facial Device New Spa High Frequency D'arsonval Home Use Device Set SNS High Frequency Home Skin Care Device with 4 Glass Electrodes Neon Darsonval Nuderma Pro NuDerma Nuderma Fusion Wand 4 pcs

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
GFE Brush, Dermabrasion, Powered General, Plastic Surgery Class 1 878.4820 2020-02-18
ISA Massager, Therapeutic, Electric Physical Medicine Class 1 890.5660 2020-02-18
NZF Static Electricity-Emitting Device, Cosmetic Use Unknown Class N N/A 2021-04-02

Official Correspondent

Ning Hu

US Agent Details

Diana Rose Anible Email: city789bird@yahoo.com Phone: (850) 5443121

Related Public Records

Same Entity

OJAN BEAUTY COMPANY LIMITED
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 3015967269. Last updated year: 2026. Please use registration number 3015967269 when referencing this establishment in official correspondence.
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