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Data / Medical devices / United States / D&M Procurement

D&M Procurement: FDA-registered device maker in Houston, TX, United States, 3 510(k) clearances

D&M Procurement is registered with the FDA (registration 3042365317) in Houston, TX, United States. It lists 4 device types. The FDA files 3 510(k) clearances under its listings, the newest dated July 9, 2025. Registered through 2026. FDA data exported November 2, 2026.

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FDA registration number
3042365317
Address
3120 Southwest Fwy Ste 101 Pmb 190944, Houston, TX, United States, 77098
Owner or operator
D&M Procurement (10094488)
Roles
Specification developer
First device listed
December 3, 2025
Registered through
2026
Brand names listed
Avina

Devices it lists

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
July 9, 2025K250193Nitrile Powder-Free Exam Gloves 2.8, Tested for Use with Chemotherapy Drugs, Opioid Fentanyl Citrate, Simulated Gastric Acid (light blue, dark blue)LZASubstantially EquivalentBasic Medical Technology, Inc.accessdata.fda.gov
February 18, 2025K243792Nitrile Powder-Free Exam Gloves Tested for Use with Chemotherapy Drugs, Opioid Fentanyl Citrate (Black,White)LZASubstantially EquivalentBasic Medical Technology, Inc.accessdata.fda.gov
January 31, 2025K243441Nitrile Powder-Free Exam Gloves Tested for Use with Chemotherapy Drugs, Opioid Fentanyl Citrate, Simulated Gastric Acid (Light blue, Dark blue)LZASubstantially EquivalentBasic Medical Technology, Inc.accessdata.fda.gov

Compare with other makers

Updated July 9, 2025. 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.