BEIJING PERFECTLASER TECHNOLOGY CO.,LTD

FDA Device Registration & Listing · Beijing, CN · Registration 3023808190

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
3023808190
FEI Number
3023808190
Entity Name
BEIJING PERFECTLASER TECHNOLOGY CO.,LTD
City/State/Country
Beijing, CN
Establishment Address
A1-1001, YANJINGZONGBUJIDI, YANJIA O AREA, Beijing 100000, CN
Establishment Type(s)
Export Device to the United States But Perform No Other Operation on Device,Manufacture Medical Device
Owner / Operator
Beijing Perfectlaser Technology Co.,Ltd (Owner Number: 10085539)
Owner / Operator Contact Address
A1-1001, YANJINGZONGBUJIDI, YANJIA O AREA, Beijing, CN-BJ 100000, CN
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

Long Pluse ND-YAG Alexandrite Laser Hair Removal System, Z110pro,Z110pro+,Z110Plus,Z110MAX,Z110MAX+ Diode Laser Hair Removal System,Z820,Z860,Z840,Z870,Z890, Lipo Laser System,W100C,W180,W180A CV80Y1,Velashape Body Shaping System,Z700pro,Z700 Multi-functional Cryolipolysis Slimming System,W680,W620,Z360 ,HIEMT Body Sculpting & Muscle Building System, ,Z950,Z900,Z940,Z940Pro,W960A,W970 ,Cavitation Slimming System,CV40C1,CV40K1, Roller Beauty System, Z710 Diode Laser Hair Removal System,Z890B,Z890C,Z890E Q-Switched Nd:YAG Laser System,Z150,Z150pro CO2 Laser Therapy SystemsZ131,Z131Pro,Z100,Z121,Z190,Z190A Hydrogen Oxygen Small Bubble System,Z400, CO2 Fractional Laser System,Z121,Z131,Z131pro,Z190,Z190A Skin/Body Analyzer Machine,W923 ,SPA Facial Beauty System,Z400 Multi-functional OPT Beauty System, Z800,Z810,Z350,

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
OHT Light Based Over-The-Counter Hair Removal General, Plastic Surgery Class 2 878.4810 2022-06-30
ORK Laser Assisted Lipolysis General, Plastic Surgery Class 2 878.4810 2022-06-30
OUP Powered Surgical Instrument For Improvement In The Appearance Of Cellulite General, Plastic Surgery Class 2 878.4790 2022-06-30
KJB Apparatus, Roller Hematology Class 1 864.2240 2022-06-30
GEX Powered Laser Surgical Instrument General, Plastic Surgery Class 2 878.4810 2025-08-20
GEX Powered Laser Surgical Instrument General, Plastic Surgery Class 2 878.4810 2025-08-20
ONG Powered Laser Surgical Instrument With MicrobeamFractional Output General, Plastic Surgery Class 2 878.4810 2024-05-21
GEX Powered Laser Surgical Instrument General, Plastic Surgery Class 2 878.4810 2024-05-21
NXF Gas, Laser Generating General, Plastic Surgery Class 1 878.4810 2022-06-30
FZZ Marker, Skin General, Plastic Surgery Class 1 878.4660 2022-06-30

Official Correspondent

No official correspondent registered.

US Agent Details

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

Related Public Records

Same Entity

Beijing Perfectlaser 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
K221336 Revelle Aesthetics, Inc. Avéli 2022-08-05
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

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
3043105515 Alovea Healthcare Co., Ltd. Suzhou Jiangsu, CN
3026132991 Shenzhen IONKA Medical Technology Co., Ltd. Shenzhen Guangdong, CN
3023272681 Shenzhen Yuwei Electronic Technology Co., Ltd. Shenzhen Guangdong, CN
3021599225 SHENZHEN BORRIA TECHNOLOGY CO.,LTD Shenzhen Guangdong, CN
3010912900 DC Altfeld - Procter & Gamble Marktheidenfeld Hesse, DE
Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3023808190. Last updated year: 2026. Please use registration number 3023808190 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.