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Data / Medical devices / China / Suzhou Beiang Smart Technology Co., Ltd

Suzhou Beiang Smart Technology Co., Ltd: FDA-registered device maker in Suzhou Jiangsu, China, 2 510(k) clearances

Suzhou Beiang Smart Technology Co., Ltd is registered with the FDA (registration 3026310685) in Suzhou Jiangsu, China. It lists 1 device type. The FDA files 2 510(k) clearances under its listings, the newest dated June 14, 2024. 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
3026310685
Address
175#, Songbei Road, Suzhou Industrial Park, Suzhou Jiangsu, China, 215000
Owner or operator
BEIANG AIR TECH LTD. (10086932)
Roles
Manufacturer
First device listed
December 23, 2022
Registered through
2026
Brand names listed
Airdog

Devices it lists

DeviceProduct codeClassRoleSource
Cleaner, Air, Medical RecirculatingFRF2Manufactureraccessdata.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
June 14, 2024K240696Airdog X8 Air Purifier (KJ800F-X8)FRFSubstantially EquivalentSuzhou Beiang Smart Technology Co., Ltd.accessdata.fda.gov
November 22, 2022K211507Airdog X5 Recirculating Air Cleaner (model KJ300F-X5)FRFSubstantially EquivalentBeiang Air Tech , Ltd.accessdata.fda.gov

Compare with other makers

Updated June 14, 2024. 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.