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Data / Medical devices / Hong Kong / Intco Medical International (hong Kong) Co., Limited

Intco Medical International (hong Kong) Co., Limited: FDA-registered device maker in Hong Kong, Hong Kong, 1 510(k) clearance

Intco Medical International (hong Kong) Co., Limited is registered with the FDA (registration 3010287987) in Hong Kong, Hong Kong. It lists 1 device type. The FDA files 1 510(k) clearance under its listings, the newest dated May 14, 2010. 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
3010287987
Address
Level 54, Hopewell Centre 183 Queens Road East, Hong Kong, Hong Kong, 12345
Owner or operator
INTCO MEDICAL INTERNATIONAL (HONG KONG) CO., LIMITED (10045823)
Roles
Manufacturer
First device listed
November 6, 2023
Registered through
2026
Brand names listed
Patient Vinyl Examination Gloves, Powder Free, Non-Sterile

Devices it lists

DeviceProduct codeClassRoleSource
Vinyl Patient Examination GloveLYZ1Manufactureraccessdata.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 14, 2010K100294SYNTHETIC POWDER-FREE VINYL PATIENT EXAMINATION GLOVESLYZSubstantially EquivalentZibo Yinghao Medical Products Co., Ltd.accessdata.fda.gov

Compare with other makers

Updated May 14, 2010. 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.