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Data / Medical devices / United States / Iv RX Pharmacy & Medical Supply Group LLC

Iv RX Pharmacy & Medical Supply Group LLC: FDA-registered device maker in Magnolia, TX, United States, 1 510(k) clearance

Iv RX Pharmacy & Medical Supply Group LLC is registered with the FDA (registration 3030086065) in Magnolia, TX, United States. It lists 1 device type. The FDA files 1 510(k) clearance under its listings, the newest dated June 20, 2014. 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
3030086065
Address
10540 FM 1488 RD PMB 140B, Magnolia, TX, United States, 77354
Owner or operator
IV RX PHARMACY & MEDICAL SUPPLY GROUP LLC (10094510)
Roles
Repackager or relabeler
First device listed
December 4, 2025
Registered through
2026
Brand names listed
NITRILE POWDER FREE EXAMINATION GLOVE - AQUA BLUE (ABLU) / VIOLET BLUE (VBLU) / DARK BLUE (DKBU)

Devices it lists

DeviceProduct codeClassRoleSource
Polymer Patient Examination GloveLZA1Repackager 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 20, 2014K140610NITRILE POWDER FREE EXAMINATION GLOVE - AQUA BLUE (ABLU) / VIOLET BLUE (VBLU) / DARK BLUE (DKBU)LZASubstantially EquivalentHartalega NGC Sdn. Bhd.accessdata.fda.gov

Compare with other makers

Updated June 20, 2014. 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.