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Data / Medical devices / United States / Inspirstar, Inc.

Inspirstar, Inc.: FDA-registered device maker in Chandler, AZ, United States, 2 510(k) clearances

Inspirstar, Inc. is registered with the FDA (registration 3005511941) in Chandler, AZ, United States. It lists 2 device types. The FDA files 2 510(k) clearances under its listings, the newest dated May 31, 2006. 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
3005511941
Address
333 N Dobson Rd Ste 5-154, Chandler, AZ, United States, 85224
Owner or operator
INSPIRSTAR, INC. (9085361)
Roles
Specification developer
First device listed
April 4, 2006
Registered through
2026
Brand names listed
INSPIRSTAR GLOVE ELECTRODE, INSPIRSTAR IS02 MIC

Devices it lists

DeviceProduct codeClassRoleSource
Electrode, CutaneousGXY2Specification developeraccessdata.fda.gov
Stimulator, Nerve, Transcutaneous, For Pain ReliefGZJ2Specification developeraccessdata.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
May 31, 2006K061343INSPIRSTAR GLOVE ELECTRODEGXYSubstantially EquivalentInspirstar, Inc.accessdata.fda.gov
March 14, 2006K060368INSPIRSTAR IS02 MICROCURRENT STIMULATORGZJSubstantially EquivalentInspirstar, Inc.accessdata.fda.gov

Compare with other makers

Updated May 31, 2006. 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.