Skip to the page

Data / Medical devices / United States / Golden Max LLC

Golden Max LLC: FDA-registered device maker in Missouri City, TX, United States, 3 510(k) clearances

Golden Max LLC is registered with the FDA (registration 1000595987) in Missouri City, TX, United States. It lists 1 device type. The FDA files 3 510(k) clearances under its listings, the newest dated June 26, 2018. 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
1000595987
Address
525 S. Cravens Rd., Suite 100, Missouri City, TX, United States, 77489
Owner or operator
Golden Max LLC (10087901)
Roles
Repackager or relabeler
First device listed
April 27, 2023
Registered through
2026
Brand names listed
Optimal

Devices it lists

DeviceProduct codeClassRoleSource
Set, Administration, IntravascularFPA2Repackager 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
June 26, 2018K173361IV Administration SetFPASubstantially EquivalentB.Braun Medical, Inc.accessdata.fda.gov
August 25, 2014K142036INFUSOMAT SPACE VOLUMETRIC INFUSION PUMP ADMINISTRATION SETSFPASubstantially EquivalentB.Braun Medical, Inc.accessdata.fda.gov
April 10, 1979K790062IV ADMINISTRATION SET WITH BACKCHECKFPASubstantially EquivalentNational Patent Development Corp.accessdata.fda.gov

Compare with other makers

Updated June 26, 2018. 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.