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Data / Medical devices / United States / Mundy Medical Marketing, Inc.

Mundy Medical Marketing, Inc.: FDA-registered device maker in Calabasas, CA, United States, 1 510(k) clearance

Mundy Medical Marketing, Inc. is registered with the FDA (registration 2028805) in Calabasas, CA, United States. It lists 2 device types. The FDA files 1 510(k) clearance under its listings, the newest dated February 13, 1990. Registered through 2026. FDA data exported November 2, 2026.

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FDA registration number
2028805
FEI number
1000135620
Address
23981 Craftsman Rd, Calabasas, CA, United States, 91302
Owner or operator
MUNDY MEDICAL, INC. (9006470)
Roles
Manufacturer, Specification developer
First device listed
January 4, 1994
Registered through
2026
Brand names listed
COOL CART, Ferkel Thigh Support, Flouro-Shield, Shoulder Holder

Devices it lists

DeviceProduct codeClassRoleSource
Medical Glove, SpecialtyLZC1Manufacturer, Specification developeraccessdata.fda.gov
Operating Room Accessories Table TrayFWZ1Manufactureraccessdata.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
February 13, 1990K893093FLOUROSHIELD RADIATION REDUCTION GLOVELZCSubstantially EquivalentAcufex Microsurgical, Inc.accessdata.fda.gov

Compare with other makers

Updated February 13, 1990. 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.