SHENZHEN KINGBRITE LIGHTING CO., LTD

FDA Device Registration & Listing · Shenzhen Guangdong, CN · Registration 3035785548

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
3035785548
FEI Number
3035785548
Entity Name
SHENZHEN KINGBRITE LIGHTING CO., LTD
City/State/Country
Shenzhen Guangdong, CN
Establishment Address
301, 8th Bldg, No.140, Guanlan Avenue, Sihe Community, Fucheng Street, Longhua District,, Shenzhen Guangdong 518110, CN
Establishment Type(s)
Manufacture Medical Device
Owner / Operator
Shenzhen KingBrite Lighting Co., Ltd (Owner Number: 10092384)
Owner / Operator Contact Address
301, 8th Bldg, No.140, Guanlan Avenue, Sihe Community, Fucheng Street, Longhua District,, Shenzhen, CN-GD 518110, CN
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

Red therapy Sleeping Bag (KB-SB), Red Therapy Light (KB-L), Red light Bed (KB-BE) Red Therapy Cap (KB-C), Beauty Led Light Mask (KB-M), Red Therapy Shoulder (KB-S), Red Therapy Neck (KB-N), Red light therapy Bar (RLB), Red light therapy Panel(RLP), Therapy Torch Red therapy Belt (KB-B), Red Therapy Knee (KB-K), Red Therapy (KB-F), Red therapy pad/ Blanket (KB-P),

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
ILY Lamp, Infrared, Therapeutic Heating Physical Medicine Class 2 890.5500 2024-12-31

Official Correspondent

Sam Yang

US Agent Details

Paddy Wong Business: ANNENG GROUP INC Email: Paddy.Wong@outlook.com Phone: (323) 9088554

Related Public Records

Same Entity

Shenzhen KingBrite Lighting Co., Ltd
View consolidated registration, premarket clearance, and recall records for this applicant.
View Entity Profile →

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3035785548. Last updated year: 2026. Please use registration number 3035785548 when referencing this establishment in official correspondence.
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