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Data / Medical devices / United States / Electromedical Technologies, Inc

Electromedical Technologies, Inc: FDA-registered device maker in Scottsdale, AZ, United States, 1 510(k) clearance

Electromedical Technologies, Inc is registered with the FDA (registration 3006791967) in Scottsdale, AZ, United States. It lists 1 device type. The FDA files 1 510(k) clearance under its listings, the newest dated July 6, 2007. Registered through 2026. FDA data exported November 2, 2026.

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FDA registration number
3006791967
Address
16413 N. 91st Street #C140, Scottsdale, AZ, United States, 85260
Owner or operator
Electromedical Technologies (10023382)
Roles
Manufacturer, Specification developer
First device listed
February 14, 2008
Registered through
2026
Brand names listed
Wellness Pro, WellnessPro Plus

Devices it lists

DeviceProduct codeClassRoleSource
Stimulator, Nerve, Transcutaneous, For Pain ReliefGZJ2Manufacturer, Specification 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
July 6, 2007K062616WELLNESSPRO 2010GZJSubstantially EquivalentIntelsource Group, Inc.accessdata.fda.gov

Compare with other makers

Updated July 6, 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.