Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3044855033

FEI Number

3044855033

Entity Name

Shenzhen Fox Hunting E-commerce Co., Ltd

City/State/Country

Shenzhen Guangdong, CN

Establishment Address

C305 Wanzhong City Clothing Wholesale Market, Xinniu Community, Minzhi Street, Longhua District, Shenzhen Guangdong 518131, CN

Establishment Type(s)

Export Device to the United States But Perform No Other Operation on Device

Owner / Operator

Shenzhen Fox Hunting E-commerce Co., Ltd (Owner Number: 10095094)

Owner / Operator Contact Address

C305 Wanzhong City Clothing Wholesale Market, Xinniu Community, Minzhi Street, Longhua District, Shenzhen, CN-GD 518131, CN

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

Eor Washer Hair removal device Hearing Aid, Air-Conduction Magnifying glass Electrified Breathing Trainer

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
OQG	Hip Prosthesis, Semi-Constrained, Cemented, Metal/Polymer, + Additive, Porous, Uncemented	Orthopedic	Class 2	888.3358	2026-01-23
OJW	Shave Prep Kit	General, Plastic Surgery	Class 2	878.4370	2026-01-23
QUF	Hearing Aid, Air-Conduction, Over The Counter	Ear, Nose, Throat	Class 1	874.3300	2026-01-23
HOI	Spectacle, Magnifying	Ophthalmic	Class 1	886.5840	2026-01-23
OGT	Oral Irrigation Kit	Dental	Class 1	872.6510	2026-01-23
ION	Exerciser, Non-Measuring	Physical Medicine	Class 1	890.5370	2026-01-23

Official Correspondent

Haisu Sun

US Agent Details

Peter Yang Business: JIAMEI CONSULTING INC. Email: info@jiameiconsulting.com Phone: (310) 2168437

Related Public Records

Same Entity

Shenzhen Fox Hunting E-commerce 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
K201660	Kyocera Medical Technologies, Inc.	KMTI Hip Replacement System, Tesera Trabecular Technologies (T3) Acetabular Shell System, Porous Acetabular Cup System	2020-07-16

Similar Registrations

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3006801265	Zhejiang Biomet Medical Products Co., Ltd.	Jinhua Zhejiang, CN
3043543260	FERRY MACHINE CORPORATION	Oakland, NJ, US
2246552	Isomedix Operations Inc.	S Plainfield, NJ, US

Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3044855033. Last updated year: 2026. Please use registration number 3044855033 when referencing this establishment in official correspondence.