Skip to the page

Data / Medical devices / China / Shenzhen Desida Technology Co., Ltd.

Shenzhen Desida Technology Co., Ltd.: FDA-registered device maker in Shenzhen Guangdong, China, 5 510(k) clearances

Shenzhen Desida Technology Co., Ltd. is registered with the FDA (registration 3015924074) in Shenzhen Guangdong, China. It lists 6 device types. The FDA files 5 510(k) clearances under its listings, the newest dated March 16, 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
3015924074
Address
5th Floor, Building A, Sanmin Industrial Zone, Shilongzai Shuitian Community, Shiyan Street, Baoan District, Shenzhen Guangdong, China, 518109
Owner or operator
Shenzhen Desida Technology Co., Ltd. (10086082)
Roles
Contract manufacturer, Manufacturer
First device listed
October 13, 2022
Registered through
2026
Brand names listed
Baby Nasal Aspirator (BN002); Baby Nasal Aspirator (BN006); Baby Nasal Aspirator (BN007); Baby Nasal Aspirator (BN008);, Baby Nasal Aspirator (BN009), Baby Nasal Aspirator (KA1006, KA1001, KA1005, NASA005, NASA006, NASA008, NASA009), Baby Nasal Aspirator,model: KA1002,KA1003,KA1012, Baby Nasal Aspirator,model: NASA011,NASA601,NASA602,NASA603,NASA605,NASA606,NASA608, Baby Nasal Aspirator,model: NASA609,NASA610,NASA012,NASA620,DQ23,BN008, Electric Nasal Aspirator (NASA601,NASA602,NASA603,NASA605,NASA606,NASA608,NASA610), Hair Removal Device (Model: IPL-D26, IPL-D19) and more

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
March 16, 2026K254079LED Light Therapy Mask (Models: T2, RLD10)OHSSubstantially EquivalentShenzhen Desida Technology Co., Ltd.accessdata.fda.gov
May 16, 2025K244033Electric Nasal Aspirator (NASA601,NASA602,NASA603,NASA605,NASA606,NASA608,NASA610)BTASubstantially EquivalentShenzhen Desida Technology Co., Ltd.accessdata.fda.gov
March 20, 2024K233901Baby Nasal Aspirator (KA1006, KA1001, KA1005, NASA005, NASA006, NASA008, NASA009)BTASubstantially EquivalentShenzhen Desida Technology Co., Ltd.accessdata.fda.gov
October 21, 2022K221643Hair Removal Device (Model: IPL-D26, IPL-D19)OHTSubstantially EquivalentShenzhen Desida Technology Co., Ltd.accessdata.fda.gov
August 31, 2022K221635IPL sapphire ice cooling hair remove deviceOHTSubstantially EquivalentShenzhen Desida Technology Co., Ltd.accessdata.fda.gov

Compare with other makers

Updated March 16, 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.