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Data / Medical devices / Singapore / Singapore Joyhub Tech Pte. Ltd.

Singapore Joyhub Tech Pte. Ltd.: FDA-registered device maker in PREMIER @ KAKI BUKT North West, Singapore, 1 510(k) clearance

Singapore Joyhub Tech Pte. Ltd. is registered with the FDA (registration 3040313889) in PREMIER @ KAKI BUKT North West, Singapore. It lists 1 device type. The FDA files 1 510(k) clearance under its listings, the newest dated May 9, 2025. Registered through 2026. FDA data exported November 2, 2026.

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FDA registration number
3040313889
Address
8 Kaki Bukit Avenue 4 #08-32, PREMIER @ KAKI BUKT North West, Singapore, 415875
Owner or operator
SINGAPORE JOYHUB TECH PTE. LTD. (10093898)
Roles
Repackager or relabeler
First device listed
July 31, 2025
Registered through
2026
Brand names listed
JOYHUB, Water soluble human lubricant, Model: JH-240ml, JH-300ml, JH-330ml, JH-20ml, JH-30ml

Devices it lists

DeviceProduct codeClassRoleSource
Lubricant, PersonalNUC2Repackager or relabeleraccessdata.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
May 9, 2025K243107Water Solubility Human Body LubricantNUCSubstantially EquivalentDongguan Yanxuan Biotechnology Co., Ltd.accessdata.fda.gov

Compare with other makers

Updated May 9, 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.