/FAQs

Frequently Asked Questions

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The iQuickIt Saliva Analyzer has been designed to provide a painless and non-invasive daily solution for people with diabetes to check their blood glucose levels using their saliva in place of traditional finger stick blood tests. Among the device’s primary objectives are for it to be accurate and reusable worldwide with little to no technical training.

At present the device is in prototype form and in the early stages of a clinical testing study. With the achievement of acceptable study results, next steps will include securing the approval of the US Food and Drug Administration (FDA).

Our ultimate goal is to provide an affordable mass produced hand held device to people with diabetes worldwide. In it’s ultimate production form, the device will be able to send blood glucose measurements real time to smart devices, where they can be shared, monitored and stored by parents, caregivers and medical professionals.

Quick, LLC, is a privately owned biomedical technology company who’s primary focus is the development of the iQuickIt Saliva Analyzer.

Please refer to our website for further information about the device, our objectives and our team.

The iQuickIt Saliva Analyzer is currently a development stage prototype and is not available for sale.

At present the device is in prototype form and in the early stages of a clinical testing study. With the achievement of acceptable study results, next steps will include securing the approval of the US Food and Drug Administration (FDA).

At this time we are not actively seeking patient volunteers. Our clinical study protocol allows only patients scheduled or requiring treatment at the study sites to be offered the opportunity to provide saliva samples for measurement and analysis by our prototype saliva analyzer device.

Please contact us if you would be interested to volunteer for future studies, as availability allows.

At the present time, the iQuickIt Saliva Analyzer is a prototype stage device and not available for sale. Thus we are not actively soliciting arrangements for distribution or marketing support.

At present the device is in prototype form and in the early stages of a clinical testing study. With the achievement of acceptable study results, next steps will include securing the approval of the US Food and Drug Administration (FDA).

Quick LLC is not actively soliciting contributions or investments at the present time.

Please contact us if you have further questions not addressed here or to let us know if you’d be interested in having us contact you in the future about your potential involvement or participation with any of the topics discussed above.