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Data / Medical devices / Vietnam / Cocomo Global Co., Ltd

Cocomo Global Co., Ltd: FDA-registered device maker in Bao Vinh Ward Dong Nai, Vietnam, 1 510(k) clearance

Cocomo Global Co., Ltd is registered with the FDA (registration 3018101395) in Bao Vinh Ward Dong Nai, Vietnam. It lists 2 device types. The FDA files 1 510(k) clearance under its listings, the newest dated May 15, 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
3018101395
Address
No.50/3, Group 26 Bao Vinh B Area, Bao Vinh Ward Dong Nai, Vietnam, 76459
Owner or operator
Cocomo Global Co., Ltd (10080898)
Roles
Contract manufacturer, Manufacturer
First device listed
April 15, 2021
Registered through
2026
Brand names listed
Bubble Overlay with air pump, Disposable Blood Pressure Cuffs

Devices it lists

DeviceProduct codeClassRoleSource
Blood Pressure CuffDXQ2Contract manufacturer, Manufactureraccessdata.fda.gov
Mattress, Flotation Therapy, Non-PoweredIKY1Manufactureraccessdata.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 15, 2015K143728Minhua Disposable Blood Pressure CuffDXQSubstantially EquivalentSuzhou Minhua Medical Apparatusaccessdata.fda.gov

Compare with other makers

Updated May 15, 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.