Nano-Photonic Purification & Sterilization

CLEAN – EFFICIENT – COMPACT - QUICK

 

 

What is Nano-Photonic Purification & Sterilization?

A unique, non-filtration process that  -

Purifies water and juices, Decontaminates air, and Sterilizes medical supplies and implants

without introducing chemicals or altering the originality of the water, juice, air or medical implement.

 

What is Nano-Photonics?

Photonics is the science of producing energy photons from light waves measured along a nanometer scale. Examples of photonics are fiber optics, lasers and solar panels.

 

What is the unique process?

The process is nano-photonic Synergistic Isogenous Active Decontamination .

 

What is ?

The  process simultaneously combines a set number of specific light waves from the same origin to eradicate harmful micro-organisms.

 

How does  eradicate micro-organisms?

The  photonic energy from the specific light waves causes the micro-organism to produce enzyme “free-radicals”. “Free-radicals” cause a dysfunctional micro-organism life process which quickly results in eradication. The public has become increasingly aware of “free-radical” science from sun block and sun screen advertising.

 

Why is  unique?

 research isolated and combined a set number (more than two) of specific light waves from trillions of light wave combinations to produce the desired effects.

 

Is  different from UV?

 is different.  UV uses a single light wave (253.7 nm) to possibly break the DNA chain within the nucleus of the micro-organism.

 

Is  safe?

Over two decades of research studies and tests by national hospitals, institutions, and universities document   use of “free-radical” science in a useful and safe format. Samplings of the studies are at http://www.synergena.com/Research.htm .

 

What is Synergena?

Synergena is the small, private research and development corporation that has conducted the  research and controls the  technology, prototypes and patents.

 

Is  FDA and EPA approved?

Being a small R&D company, Synergena has focused resources on the studies and testing of  technology and devices. Although  devices were successfully tested in accordance with FDA and EPA criteria, additional legal and capital resources are necessary for regulatory agency approvals.

 

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