As part of its goal to reduce post-operative drug
dependence, innovative biotechnology company Endonovo Therapeutics (OTCQB: ENDV) recently revealed
plans to get its flagship SofPulse Therapy Device into 600 hospitals within the
next 18 months. An article further discussing the company reads, “On June 13,
the company detailed its initial strategy for a national rollout of its
SofPulse targeted pulsed electromagnetic field (tPEMF) therapy device to
hospitals throughout the United States. According to the company’s news
release, Endonovo plans to be in the evaluation stage with 600 hospitals within
the next 18 months, employing 300 sales representatives (http://ibn.fm/gAHv2). . . .
‘After careful consideration and discussions, and in accordance with our
internal budgets, we have reached the point at which we can confidently
announce our national rollout plan and strategy,’ CEO Alan Collier stated in a
new release. ‘We believe, based on numerous meetings with doctors and hospital
administrators, the level of acceptance of our SofPulse device supports our
plans to be in hospitals throughout all 50 states by 2020. With the public
demanding change and options other than opioids, and with very few alternatives
to satisfy those demands, SofPulse is a natural and safe replacement to opioids
and a solution to this health crisis.’”
To view the full article, visit http://ibn.fm/SWep8
About Endonovo Therapeutics Inc.
Endonovo Therapeutics is a commercial-stage developer of
noninvasive wearable electroceuticals(TM) therapeutic devices. The company’s
current portfolio of commercial and clinical-stage wearable electroceuticals
therapeutic devices addresses wound healing, pain, postsurgical pain and edema,
cardiovascular disease, chronic kidney disease and central nervous system
(“CNS”) disorders including traumatic brain injury (“TBI”), acute concussions,
postconcussion syndrome and multiple sclerosis. The company’s noninvasive
electroceutical therapeutic device, SofPulse(R), using pulsed short-wave
radiofrequency at 27.12 MHz, has been FDA cleared and CE marked for the
palliative treatment of soft-tissue injuries and postoperative pain and edema,
and has CMS national coverage for the treatment of chronic wounds. The
company’s current portfolio of preclinical-stage electroceuticals therapeutic
devices addresses chronic kidney disease, liver disease nonalcoholic
steatohepatitis (“NASH”), cardiovascular and peripheral artery disease (“PAD”),
and ischemic stroke. The company’s noninvasive, wearable electroceuticals
therapeutic devices work by restoring key electrochemical processes that
initiate anti-inflammatory and growth-factor cascades necessary for healing to
occur. For more information, visit the company’s website at www.Endonovo.com.
NOTE TO INVESTORS: The latest news and updates
relating to ENDV are available in the company’s newsroom at http://ibn.fm/ENDV
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