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Data / Medical devices / United States / Azure Microdynamics, Inc.

Azure Microdynamics, Inc.: FDA-registered device maker in Foothill Ranch, CA, United States, 1 510(k) clearance

Azure Microdynamics, Inc. is registered with the FDA (registration 3007279910) in Foothill Ranch, CA, United States. It lists 1 device type. The FDA files 1 510(k) clearance under its listings, the newest dated January 26, 1994. Registered through 2026. FDA data exported November 2, 2026.

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FDA registration number
3007279910
Address
19652 Descartes, Foothill Ranch, CA, United States, 92610
Owner or operator
Azure Microdynamics, Inc. (10027145)
Roles
Manufacturer
First device listed
October 7, 2008
Registered through
2026
Brand names listed
VECS Palate Expander

Devices it lists

DeviceProduct codeClassRoleSource
Bracket, Metal, OrthodonticEJF1Manufactureraccessdata.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
January 26, 1994K926427LARIAT PALATE EXPANDEREJFSubstantially EquivalentEasy Access Orthodontics, Inc.accessdata.fda.gov

Compare with other makers

Updated January 26, 1994. 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.