Skip to the page

Data / Medical devices / China / Nanjing Bestview Laser S&T Co.,ltd.

Nanjing Bestview Laser S&T Co.,ltd.: FDA-registered device maker in Nanjing Jiangsu, China, 7 510(k) clearances

Nanjing Bestview Laser S&T Co.,ltd. is registered with the FDA (registration 3021011208) in Nanjing Jiangsu, China. It lists 2 device types. The FDA files 7 510(k) clearances under its listings, the newest dated May 7, 2026. Registered through 2026. FDA data exported November 2, 2026.

SpecStream is the live web data engine for teams and agents. It reads the FDA registration and listing, 510(k), PMA, recall and enforcement files from openFDA every week, and this page is that reading, joined by the FDA's own numbers. Ask for the makers of any device type in any country and new clearances, approvals and recalls arrive in your sheet, CRM, Slack or agent as the FDA publishes them.

FDA registration number
3021011208
Address
1st & 2nd Floor,Building 5,Liandong U Valley Science and Technology Innovation Park,No.1 Hengyi Road,Nanjing, Nanjing Jiangsu, China, 210000
Owner or operator
Nanjing Bestview Laser S&T Co.,Ltd. (10086603)
Roles
Manufacturer
First device listed
November 23, 2022
Registered through
2026
Brand names listed
CO2 Laser Machine, CO2 Laser Machine ( Model: Monica-I, Monica-II ), CO2 Laser Machine(Lume), Diode Laser Machine, Intense Pulsed Light Treatment System, Q-Switched Nd:YAG Laser System, Thulium Laser System (Deluxlase)

Devices it lists

510(k) clearances

The 510(k) numbers this establishment lists, with the FDA decision on each. The applicant is the company that holds the clearance.

Decided510(k) numberDeviceProduct codeDecisionApplicantSource
May 7, 2026K260974CO2 Laser Machine (Monica-I,Monica-II)GEXSubstantially EquivalentNanjing Bestview Laser S&T Co., Ltd.accessdata.fda.gov
April 20, 2026K260153Q-Switched Nd: YAG Laser System (Glamor Q)GEXSubstantially EquivalentNanjing Bestview Laser S&T Co., Ltd.accessdata.fda.gov
September 26, 2025K251919Thulium Laser System (Deluxlase)GEXSubstantially EquivalentNanjing Bestview Laser S&T Co., Ltd.accessdata.fda.gov
June 9, 2025K250465CO2 Laser Machine (Lume)GEXSubstantially EquivalentNanjing Bestview Laser S&T Co., Ltd.accessdata.fda.gov
November 14, 2024K242440Intense Pulsed Light Treatment System (LK-PT)ONFSubstantially EquivalentNanjing Bestview Laser S&T Co., Ltd.accessdata.fda.gov
October 22, 2021K211735CO2 Laser Machine, Model: BW-203BGEXSubstantially EquivalentZhengzhou Bestview ST Co., Ltd.accessdata.fda.gov
July 28, 2021K211335Diode Laser Machine, Model Number: BM-100GEXSubstantially EquivalentZhengzhou Bestview ST Co., Ltd.accessdata.fda.gov

Compare with other makers

Updated May 7, 2026. Read from openFDA bulk downloads (device registration and listing, 510(k), PMA, recall and enforcement files). CC0 1.0, public domain (openFDA terms of service). The files are joined on FDA identifiers: the 510(k) and PMA numbers a registration lists, and the recalling firm's FEI for recalls. Recall class comes from the FDA enforcement report. The FDA states that openFDA data is unvalidated and is not for decisions about medical care. Free to reuse with credit to SpecStream under CC BY 4.0. Spot a wrong value? Write to [email protected] with the link to this page.