Skip to the page

Data / Medical devices / China / Shenzhen Rainbow Technology Co.,ltd

Shenzhen Rainbow Technology Co.,ltd: FDA-registered device maker in Shenzhen Guangdong, China, 2 510(k) clearances

Shenzhen Rainbow Technology Co.,ltd is registered with the FDA (registration 3018994966) in Shenzhen Guangdong, China. It lists 12 device types. The FDA files 2 510(k) clearances under its listings, the newest dated January 23, 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
3018994966
Address
3rd Floor, No.2, Dongwangyang Industry, Huangtian Community Hangcheng Street, Bao'an District, Shenzhen Guangdong, China, 518000
Owner or operator
Shenzhen Rainbow Technology Co.,Ltd (10087485)
Roles
Exporter to the US, Manufacturer
First device listed
March 5, 2023
Registered through
2026
Brand names listed
Dreame Cold Pack, Electronic nail files, RB-015, RB-015B, RB-015C, RB-015D,RB-015F, RB-015G, Eye massager, Eye beauty device, RB-017, RB-017B, RB-017C, RB-017D, LED Face Mask, LED Therapy Mask,LED Facial mask,4D Face mask,4D Facial mask,, LED Light Therapy Mask (Model(s): RB-008, RB-030, RB-081, RB-008G, RB-008GB, RB-008J, RB-008JB), LED Light Therapy Mask (Model: RB-030), LED Light Therapy Mask, LED mask, GLOW Therapy LED Mask, LED Therapy Red Light Mask, LED Face Mask,, LED Light Therapy Mask,LED mask, GLOW Therapy LED Mask, LED Therapy Red Light Mask, 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
January 23, 2026K253712LED Light Therapy Mask (RB-051, RB-061, RB-071, RB-052, RB-062, RB-072, RB-053, RB-063, RB-073)OHSSubstantially EquivalentShenzhen Rainbow Technology Co., Ltd.accessdata.fda.gov
January 28, 2025K243423LED Light Therapy Mask (Model(s): RB-008, RB-030, RB-081, RB-008G, RB-008GB, RB-008J, RB-008JB)OHSSubstantially EquivalentShenzhen Rainbow Technology Co., Ltd.accessdata.fda.gov

Compare with other makers

Updated January 23, 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.