Endonovo Therapeutics (OTCQB: ENDV) today announced
that it has secured sales of SofPulse(R), the company’s FDA-Cleared,
non-invasive device utilized for the reduction of postoperative pain and edema,
to multiple plastic surgery centers. “SofPulse(R) main distribution model is
marketing to major hospitals throughout the US and is beginning to be viewed as
the standard of care for postoperative pain and edema reduction for numerous
inpatient hospital procedures. With the expansion of our customer base and
recent orders from numerous plastic surgery centers, SofPulse(R) demonstrates
different applications for its use,” Endonovo Therapeutics CEO Alan Collier
stated in the news release. “We are quickly becoming the go to pain and edema
reduction option for many out-patient surgical procedures performed at ASC’s
throughout the US. These centers provide patients with cosmetic and
reconstructive procedures resulting in a need for postoperative pain
management. Many of the plastic surgery centers have state-of-the-art surgical
suites and recovery rooms equipped to hospital standards and we continue
working with these centers and completing evaluations. Although in the nascent
stages of expanding into fully certified office-based surgery centers, we
recognize the large and growing market size allowing us to be well poised to
capitalize on this opportunity.”
To view the full press release, visit http://ibn.fm/XFQEg
About Endonovo Therapeutics
Endonovo Therapeutics, Inc. is a commercial-stage developer
of noninvasive wearable Electroceuticals(R) therapeutic devices. The Company’s
current portfolio of commercial and clinical-stage wearable Electroceuticals(R)
therapeutic devices addresses wound healing, pain, post-surgical pain and
edema, cardiovascular disease, chronic kidney disease, and central nervous
system (“CNS”) disorders, including traumatic brain injury (“TBI”), acute
concussions, post-concussion syndrome and multiple sclerosis. The Company’s
noninvasive Electroceutical(R) therapeutic device, SofPulse(R), which uses
pulsed short-wave radiofrequency at 27.12 MHz, has been FDA-cleared and CE
marked for the palliative treatment of soft tissue injuries and post-operative
pain and edema and has CMS national coverage for the treatment of chronic
wounds. The Company’s current portfolio of preclinical-stage
Electroceuticals(R) therapeutic devices addresses chronic kidney disease, liver
disease non-alcoholic steatohepatitis (“NASH”), cardiovascular and peripheral
artery disease (“PAD”), and ischemic stroke. The Company’s noninvasive,
wearable Electroceuticals(R) 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 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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