Rapid Point-of-Care

COVID-19 Testing

in Fountain Hills, AZ

Rapid Point-of-Care

COVID-19 Testing

in Fountain Hills, AZ

Covid-19 Testing Prices

Results within 24 Hours


Results within 45 Minutes


Payments accepted with cash or credit card.

Convenient and Accurate Covid-19 Testing Solutions

Quick, Reliable Coronavirus Testing in Fountain Hills, AZ

Welcome to DI+ Lab, your friendly community lab, providing cutting edge technology and solutions to serving local neighborhoods with trusted and well-trained professionals and lab technicians.

  • Get COVID-19 and or Influenza test results within 30-45 minutes
  • FDA EUA Approved - CLIA certification 03D2190861
  • Supporting healthcare, schools, workplaces with rapid testing. We can develop programs to administer rapid same day COVID-19 and Influenza test results to secure your workplace, school, hospital, and events.

Methods Of Testing

Quidel Sofia SARS Antigen

IFA has been granted Emergency Use Authorization (EUA) by the FDA This has been issued for the manufacturer Quidel Corporation (Quidel) antigen detection tests—the Sofia SARS Antigen FIA and Influenza(Flu) Type A and B. These assays are approved for detection of the nucleocapsid protein antigen from SARS-CoV-2 in nasal and nasopharyngeal swab specimens and authorized for use by laboratories certified under the Clinical Laboratory Improvement Amendments of 1988 (CLIA), 42 U.S.C. § 263a, which meets the requirements to perform waived, moderate, or high complexity tests. Quidel announced on July 17, 2020, that it updated the performance data for this test to 96.7% using direct nasal swab specimens versus Polymerase Chain Reaction (PCR) test as a result of further studies included in its amended EUA that were submitted to the FDA.

ID Now™ COVID-19

Authorized by the FDA under an emergency use authorization for use by authorized laboratories and patient care settings. The test has been authorized only for the detection of nucleic acid from SARS-CoV-2, and is only authorized for the duration of the declaration that circumstances exist justifying the authorization of emergency use of in vitro diagnostic tests for detection and/or diagnosis of COVID-19 under Section 564(b)(1) of the Act, 21 U.S.C. § 360bbb-3(b)(1

TECHNOLOGY — ID NOW™ utilizes proven isothermal molecular technology in an intuitive platform, providing the fastest molecular results in the market1

Coming Soon

DI+ can deploy dedicated healthcare and lab professionals along with state-of-the-art testing technology where you are located.

DI+ also provides service contracts with both on-demand and subscription services.

Download This Guide

To Help You Understand How COVID-19 Testing Works

Slow The Spread

With these easy steps


Wash Your Hands Often


Cover Your Face With A Mask


Keep Social Distance


Clean and Disinfect


Stay Home When Possible

Step One

Request your appointment time that best fits your schedule.

Step Two

Come to the Diagnostics Institute Plus offices to get your sample collected.

Step Three

Receive your rapid COVID-19 test results within 45 minutes.


Follow these simple steps when visiting Diagnostic Institute Plus

  1. Make an appointment/sign up online for the time to come in.
  2. Registration online: Name, DOB, email address, cell phone number, physical address, ethnicity
  3. Arrive 10 minutes before your appointment and wait in the car. Message or call us when you arrive. When it is your turn you will get a text to come in. If you have active symptoms, please call 480-508-5355 to let us know.
  4. Walk up to the office with a mask on. At the counter be prepared to show your ID, and confirm the spelling of your name, date of birth, and confirm which test you are purchasing. Then a swab sample will be obtained.
  5. You leave immediately and wait in your car. We will let you know when you can go. Your test results will be sent to you via secure text message/email address in 30-45 minutes or within 24 hours depending on the test you purchased.

Have Questions About COVID-19 Testing?

We've answered some of the most frequently asked questions that we have received about rapid COVID-19 testing.

The ID NOW COVID-19 test is a rapid, molecular point-of-care test that detects COVID-19 in 13 minutes or less. It is used on our ID NOW platform. Abbott received emergency use authorization (EUA) from the U.S. Food and Drug Administration (FDA) for the ID NOW COVID-19 test in March 2020. ID NOW is an FDA approved CLIA-waived instrument, which means that the technology can be used in settings outside the traditional hospital setting. Healthcare professionals using ID NOW should be trained on how to use the instrument.

This article helps explain how the ID NOW molecular point-of-care test for COVID-19 works. Learn more.

Results may be delivered in 13 minutes or less.

Our ID NOW molecular point-of-care test met all testing criteria in the FDA's emergency use authorization (EUA) and we’re continuing to collect more clinical data in the field. The ID NOW instrument uses molecular technology and molecular tests, in general, are valued for their high level of accuracy in similar settings such as flu testing. Learn more.

The direct swab method is the best way to ensure the test performs as expected.

To optimize results, do not use viral transport media (VTM), which could reduce the sensitivity of the test through dilution. Learn more.

Don't see your question answered? Please contact us at 480-508-5355 and we'll be in touch with you as soon as possible.


Fountain Hills' Premier COVID-19 Testing Services

Questions or Comments?

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