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Data / Medical devices / China / Solid Toys Ind. Ltd.

Solid Toys Ind. Ltd.: FDA-registered device maker in Boluo County, Huizhou,City Guangdong, China, 1 510(k) clearance

Solid Toys Ind. Ltd. is registered with the FDA (registration 3004529379) in Boluo County, Huizhou,City Guangdong, China. It lists 8 device types. The FDA files 1 510(k) clearance under its listings, the newest dated May 24, 2013. 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
3004529379
Address
No. 274 Mingyue Third Road Tie Chang Industrial Zone, Shiwan Town, Boluo County, Huizhou,City Guangdong, China, 518120
Owner or operator
SOLID TOYS IND. LTD. (9062739)
Roles
Contract manufacturer, Manufacturer, Specification developer
First device listed
April 13, 2004
Registered through
2026
Brand names listed
Bunny ASPIRATOR, Finger toothbrush gum massager, MEDICAL DROPPER, Manual toothbrush, Medical dispenser, Medical spoon, NUK Reusable Nursing Pads, NUK cool critter 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
May 24, 2013K123855WATER-FILLED TEETHERKKOSubstantially EquivalentSolid Toys Ind. , Ltd.accessdata.fda.gov

Compare with other makers

Updated May 24, 2013. 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.