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Thursday, 11/01/2018 5:50:41 PM

Thursday, November 01, 2018 5:50:41 PM

Post# of 69950
I'm extremely encouraged by Innerscope's latest PR. It seems that Mark and Matthew have both been very involved with Erchonia for sometime given their "resolute optimism" of what Erchonia's tech can do for the hearing impaired. It also seems like they've already gotten engineering underway for product development from research that has ALREADY HAPPENED. The FDA 510k requires a 90-day notice, which means they have to submit for product marketing for FDA approval between 9/2 and 10/1 of 2019 to hit their December mark. (SIDENOTE: CAN'T WAIT TO SEE THEIR 10Q TO SEE WHERE THEY SIT WITH THEIR NOTES)

https://www.fda.gov/medicaldevices/productsandmedicalprocedures/deviceapprovalsandclearances/510kclearances/

'"Our long-term partnership with the Erchonia, the world leader in 3LT research and technology, has resulted in the first of many opportunities to serve the hearing impaired," said Matthew Moore, CEO of InnerScope Hearing Technologies. "We are confident in a successful clinical outcome using Erchonia's 3LT technology to treat Hearing Disorders. Our Chairman, Mark Moore, has invested critical resources in assisting Erchonia in the development of these Hearing Products, and has witnessed the possibilities with resolute optimism. Once our tinnitus treatment receives the 510k FDA Market Clearance, we plan to market and distribute this worldwide to help the hundreds of millions of people who suffer from tinnitus. InnerScope and Erchonia also intends to obtain more 510k FDA-Clearances by developing more treatment applications for other Hearing Disorders using Erchonia's 3LT technology," Mr. Moore concluded.'

And then there they go...tugging at heartstrings across America...

'In addition, InnerScope plans on working with U.S. Department of Veterans Affairs for using its hearing products for treating the millions of U.S. veterans that suffer from tinnitus.'

Well played IMO. :)