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Data / Medical devices / United States / Good Methods Global Inc.

Good Methods Global Inc.: FDA-registered device maker in Celebration, FL, United States, 1 510(k) clearance

Good Methods Global Inc. is registered with the FDA (registration 3043840131) in Celebration, FL, United States. It lists 1 device type. The FDA files 1 510(k) clearance under its listings, the newest dated March 13, 2026. Registered through 2026. FDA data exported November 2, 2026.

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FDA registration number
3043840131
Address
2954 Mallory Cir Ste 209, Celebration, FL, United States, 34747
Owner or operator
Good Methods Global Inc. (10095496)
Roles
Manufacturer
First device listed
March 20, 2026
Registered through
2026
Brand names listed
Aeka Imaging; TigerView 2; TigerViewX

Devices it lists

DeviceProduct codeClassRoleSource
System, Image Processing, RadiologicalLLZ2Manufactureraccessdata.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
March 13, 2026K253111Aeka ImagingLLZSubstantially EquivalentGood Methods Global, Inc.accessdata.fda.gov

Compare with other makers

Updated March 13, 2026. 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.