Titan Medical Inc (TMDIF)

[66Mustang]

That Mass Device article is rather dated at this point; lots of changes since then. Here's a sampling for your perusal.

Some great stuff in here as it could apply to Titan...
https://www.medtechdive.com/news/medtronic-earnings-call-coronavirus-updates/578498/
But Hugo is delayed; as of May they could not piece a new timeline together.

This next one shows original Hugo was planned for sale in 2022, but is delayed. It also indicates Titan tech to be used in Hugo, which is new news... Means Hugo IS being re-designed with our tech, so the 2022 release could easily be moved to 2024, and therefore they need Enos ASAP to get in the market. And it is SO convenient that they have COVID to blame for their need to re-design Hugo with our tech. No judgment here... I don't blame them!
https://www.medicaldevice-network.com/deals-analysis/medtronic-titan/

Further evidence their earlier plans were more aggressive:
https://vfrsi.vattikutifoundation.com/medtronic-hugo-

This one is funny, Titan pays Medtronic $10M??? They got it backwards!
https://www.therobotreport.com/titan-medica-medtronic-sign-surgical-robotics-development-agreements/

CMR's is another MegaBot; multi-pod floor hog. No worries here as far as competition for Titan (or Enos, for whoever markets it).
https://www.medicaldevice-network.com/features/da-vinci-surgical-robot-competitors/

Lots happening! It all looks GREAT for Titan and its shareholders!

Whats funny is all the recent articles I found, none of them say anything bad about Titan or our NASDAQ status or our Management team... Just nothing bad! So if you do hear bad things about Titan, ask for published references and you probably won't get them.



Message in reply to:
This is what I was saying.....

Maybe clinical trials won't be around Chapel Hill.They will ship robots to India for human trials.Shh......

Medtronic plans to launch the Hugo system in undisclosed places outside the U.S. early the next year, allowing the company to start gathering clinical data, White said. CE Mark and U.S. IDE submissions will follow later in the year, with a goal of achieving U.S. 510(k) clearance in about two years.

https://www.massdevice.com/medtronic-finally-unveils-its-new-robot-assisted-surgery-system/