Not sure how caught up you are with everything, but two Mayo Clinic doctors who have been working closely with Vivos Inc for a few years now also have been attending the FDA meetings to help them answer question as well as advocate for the need of Radiogel. Mayo Clinic has agreed to preform the human trials if they receive the IDE approval.
I wonder if that is acknowledging the time passed since they gave the test plan to Mayo clinic doctors to review. Given the time that has passed and this statement it seems Vivos first draft needed a lot of revision before putting it in front of the FDA. Hope this means the revision is over and soon we will hear about another FDA meeting.
With the tweet this morning, it sounds like we're past the rabbit test, and waiting for the FDA to give us the go ahead on Human trials. We wouldn't be be discussing the future this far ahead if there were problems with our recent tests and the FDA. Just my thoughts .