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Data / Medical devices / Malaysia / Kin Yat Industrial (malaysia) Sdn. Bhd.

Kin Yat Industrial (malaysia) Sdn. Bhd.: FDA-registered device maker in Senai Johor, Malaysia, 1 510(k) clearance

Kin Yat Industrial (malaysia) Sdn. Bhd. is registered with the FDA (registration 3038613158) in Senai Johor, Malaysia. It lists 1 device type. The FDA files 1 510(k) clearance under its listings, the newest dated February 24, 2015. 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
3038613158
Address
PLO44, Jalan Perindustrian Senai, Kawasan Perindustrian Senai Fasa 2, Senai Johor, Malaysia, 81400
Owner or operator
KIN YAT INDUSTRIAL (MALAYSIA) SDN. BHD. (10093451)
Roles
Manufacturer
First device listed
May 17, 2025
Registered through
2026
Brand names listed
MOTIF ROAM BREAST PUMP, MOTIF ROAM STARTER KIT, MOTIF TWIST BREAST PUMP, MOTIF TWIST STARTER KIT

Devices it lists

DeviceProduct codeClassRoleSource
Pump, Breast, PoweredHGX2Manufactureraccessdata.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
February 24, 2015K142479MEGNA BREAST PUMPSHGXSubstantially EquivalentWuxi Xinzhongrui Baby Supplies Co., Ltd.accessdata.fda.gov

Compare with other makers

Updated February 24, 2015. 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.