Foshan Haiseer Electronic Technology Co., Ltd.

FDA Device Registration & Listing · Foshan Guangdong, CN · Registration 3043729119

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
3043729119
FEI Number
3043729119
Entity Name
Foshan Haiseer Electronic Technology Co., Ltd.
City/State/Country
Foshan Guangdong, CN
Establishment Address
Room 701-1, Building 3, Youchuang Intelligent Manufacturing Park, No. 9 Libo Road, Shishan Town, Nanhai District, Foshan Guangdong 528000, CN
Establishment Type(s)
Manufacture Medical Device
Owner / Operator
Foshan Haiseer Electronic Technology Co., Ltd. (Owner Number: 10095184)
Owner / Operator Contact Address
Room 701-1, Building 3, Youchuang Intelligent Manufacturing Park, No. 9 Libo Road, Shishan Town, Nanhai District, Foshan, CN-GD 528000, CN
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
K233556
PMA Number
N/A

All Registered Proprietary Names

PDTVERA CurrentBody Skin RF Device (ST030) Diode Laser Therapy Systems Laser Hair Growth Cap (Model:TW080) RED Light Therapy Underwear Therapeutic Chiropractic Massager, Model: 3068 PDTVERA LED Eye mask (Model: EY-20R)

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
PAY Over-The-Counter Radiofrequency Coagulation Device For Wrinkle Reduction General, Plastic Surgery Class 2 878.4420 2026-04-07
GEX Powered Laser Surgical Instrument General, Plastic Surgery Class 2 878.4810 2026-02-20
OAP Laser, Comb, Hair Physical Medicine Class 2 890.5500 2026-05-22
ILY Lamp, Infrared, Therapeutic Heating Physical Medicine Class 2 890.5500 2026-02-04
ISA Massager, Therapeutic, Electric Physical Medicine Class 1 890.5660 2026-03-13
OHS Light Based Over The Counter Wrinkle Reduction General, Plastic Surgery Class 2 878.4810 2026-06-04

Official Correspondent

Dongliang Xue

US Agent Details

Dennis Lee Email: FoshanHeisel@outlook.com Phone: (614) 5308929

Related Public Records

Same Entity

Foshan Haiseer Electronic Technology 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
K083258 Dornier Medtech America, Inc. MEDILAS D FAMILY LASERS, INCLUDING MEDILAS D LITEBEAM, LITEBEAM +, UROBEAM, MULTIBEAM, FLEXIPULSE AND MAGNAPULSE 2009-01-30
K201111 Candela Corporation GentleMax Pro Plus 2020-05-26
K202758 Shangdong Huamei Technology Co., Ltd. Nd: YAG Laser Therapy Systems HM-YL900 2020-11-16
K904068 Luxar Corp. LUXAR MODEL LX-20 CO2 LASER 1991-04-15
K142225 CAO Group, Inc. Pilot Elite Diode Laser 2014-09-12

Related Recall Records

Recall ID Recalling Firm Recall Class Product Description
Z-0005-2014 PhotoMedex, Inc. 2
The product is labeled in part "***Surgical Laser Technologies, Inc. Montgomeryville, PA***SLT Fiber Delivery System***Sterile***Non-Pyrogenic***. The product is packaged in a flexible pouch and includes the following laser surgery accessories - SLT-SSRH 8, Catalog/Product Number 0041-3082; SLT-SSRH 11, Catalog/Product Number 0041-3112; SLT-SSRH 4-SMA, Catalog/Product Number 0042-0075; SLT-SSRH 5-SMA, Catalog/Product Number 0042-0076; SLT-SSRH 6-SMA, Catalog/Product Number 0042-0077; SLT-SSRH 7-SMA, Catalog/Product Number 0042-0078; SLT-SSRH 8-SMA, Catalog/Product Number 0042-0079; SLT-SSRH 9-SMA, Catalog/Product Number 0041-4931; and SLT-SSRH 10-SMA, Catalog/Product Number 0042-0081. Indicated for the incision, excision, coagulations, and vaporization of soft tissue.
Z-0025-2018 Medtronic Navigation, Inc. 2
VCLAS (Visualase Cooled Laser Ablation System) Part Number: 9735559 Visualase Cooled Laser Applicator System 3mm Tip; Part Number: 9735560 Visualase Cooled Laser Applicator System 10mm Tip; Part Number: 9735561 Visualase Cooled Laser Applicator System 15mm Tip
Z-0028-2007 Lumenis Inc. 2
Lumenis brand DuoTome SideLite 550 Micron Delivery System; laser systems for ablating soft tissue. Catalog Number: 0641-800-01; Manufactured by Lumenis, Inc., 2400 Condensa Street, Santa Clara, CA

Similar Registrations

Registration Number Establishment Name Location
3017132875 BEIJING SPIRITLASER SCIENCE & TECHNOLOGY CO., LTD. Beijing, CN
3007048256 QUASAR ENGINEERING LTD. Kowloon, HK
3027645761 SILK'N BEAUTY LTD. Rotterdam Zuid-Holland, NL
3012104022 FOREO INC Las Vegas, NV, US
3016076077 VIS (SHANGHAI) TECHNOLOGY CO., LTD. Jinshan District Shanghai, CN
Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3043729119. Last updated year: 2026. Please use registration number 3043729119 when referencing this establishment in official correspondence.
Legal Disclaimer: AvaSpecs is not affiliated with the FDA or any government agency and does not provide medical, legal, regulatory, safety, approval, clearance, effectiveness, endorsement, or compliance advice. This index page is built using public record archives and does not represent an official regulatory determination.
Account Required Full available specs will require a free AvaSpecs account.