Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3005912219

FEI Number

3005912219

Entity Name

Shenzhen reanson products co.,ltd.

City/State/Country

SHENZHEN Guangdong, CN

Establishment Address

No.16, 3rd ind zone, xia village, gongming town, guangming district, SHENZHEN Guangdong 518106, CN

Establishment Type(s)

Manufacture Medical Device

Owner / Operator

Shenzhen reanson products co.,ltd (Owner Number: 9091407)

Owner / Operator Contact Address

No.16, 3rd ind zone, xia village, gongming town, guangming district, Shenzhen, CN-GD 518106, CN

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

Helmet Non medical mask Non medical protective clothing Swimming goggles; diving mask; safety goggles; ski goggles ; sunglasses; motorcycle goggles Non medical protective glasses

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
NDA	Helmet, Cranial, For Protective Use	Physical Medicine	Class 1	890.3025	2020-04-04
MSH	Respirator, Surgical	General, Plastic Surgery	Class 2	878.4040	2022-08-04
OEA	Non-Surgical Gown	General, Plastic Surgery	Class 1	878.4040	2020-04-04
HOY	Shield, Eye, Ophthalmic (Including Sunlamp Protective Eyewear And Post-Mydriatic Eyewear)	Ophthalmic	Class 1	886.4750	2020-04-04

Official Correspondent

Iris Lau

US Agent Details

Yueting Zhu Business: SOUTH BAY INNOVATION LLC Email: southbayinnovation@southbayinnovation.com Phone: (424) 3769142

Related Public Records

Same Entity

Shenzhen reanson products 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
K102092	Prestige Ameritech	PRO GEAR N95 PARTICULATE FILTER RESPIRATOR & SURGICAL MASK, REGULAR SIZE MODEL RP CERIES	2010-10-06

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3005912219. Last updated year: 2026. Please use registration number 3005912219 when referencing this establishment in official correspondence.