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Data / Medical devices / United States / Zebra Technologies Corporation

Zebra Technologies Corporation: FDA-registered device maker in Morris Plains, NJ, United States, 1 510(k) clearance

Zebra Technologies Corporation is registered with the FDA (registration 3004437723) in Morris Plains, NJ, United States. It lists 2 device types. The FDA files 1 510(k) clearance under its listings, the newest dated August 15, 2007. 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
3004437723
Address
116 American Rd., Morris Plains, NJ, United States, 07950
Owner or operator
TEMPTIME Corporation (10022589)
Roles
Manufacturer
First device listed
October 5, 2007
Registered through
2026
Brand names listed
HEATmarker TTI, Safe-T-Vue

Devices it lists

DeviceProduct codeClassRoleSource
Indicator, Physical/Chemical, Storage TemperatureOCI2Manufactureraccessdata.fda.gov
Supplies, Blood-BankKSS1Manufactureraccessdata.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
August 15, 2007K063759HEATMARKER TIME TEMPERATURE INDICATOROCISubstantially EquivalentTemptime Corporationaccessdata.fda.gov

Compare with other makers

Updated August 15, 2007. 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.