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Data / Medical devices / China / Shenzhen Beacon Display Technology Co., Ltd.

Shenzhen Beacon Display Technology Co., Ltd.: FDA-registered device maker in Shenzhen Guangdong, China, 3 510(k) clearances

Shenzhen Beacon Display Technology Co., Ltd. is registered with the FDA (registration 3009553444) in Shenzhen Guangdong, China. It lists 2 device types. The FDA files 3 510(k) clearances under its listings, the newest dated October 29, 2025. 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
3009553444
Address
Floor1-4,Building 6,Hualian Industrial Zone, Hualing Road, Dalang Community, Longhua District, Shenzhen Guangdong, China, 518109
Owner or operator
Shenzhen Beacon Display Technology Co., Ltd. (10045984)
Roles
Complaint file establishment, Manufacturer
First device listed
November 1, 2020
Registered through
2026
Brand names listed
3MP Color LCD Monitors C310S, C316S; 3MP Monochrome LCD Monitors G310S, G316S; 6MP Color LCD Monitor C616W., 4MP/8MP Color LCD Monitors C44W+/C82W+, C83W+, C85W+, C822W, E190, E2420, E2421, E2422, S2421P, S2720P, S271P, S3221P, S3221P-3D, S421, S2785P, E2120, E2121, S2780P, S3281P, S3282P, S3285P, S3286P, S3285P-3D, S4385P, S5583P, SP2421T, SP5581P, SP5581T

Devices it lists

DeviceProduct codeClassRoleSource
Camera, Surgical And AccessoriesKQM1Complaint file establishment, Manufactureraccessdata.fda.gov
Display, Diagnostic RadiologyPGY2Complaint file establishment, Manufactureraccessdata.fda.gov

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
October 29, 2025K253242LCD Monitor (C1216W, C822W, C821W)PGYSubstantially EquivalentShenzhen Beacon Display Technology Co., Ltd.accessdata.fda.gov
October 25, 2024K243031LCD Monitors C310S, G310S, C316S, G316S, C616WPGYSubstantially EquivalentShenzhen Beacon Display Technology Co., Ltd.accessdata.fda.gov
October 19, 2020K2023744MP/8MP Color LCD Monitors C44W+/C82W+, C83W+, C85W+PGYSubstantially EquivalentShenzhen Beacon Display Technology Co., Ltd.accessdata.fda.gov

Compare with other makers

Updated October 29, 2025. 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.