Asensus Surgical Provides Preliminary 2021 Year-End Corporate Update
Asensus Surgical (AMEX: ASXC) reported significant growth in its preliminary 2021 year-end update. The company performed over 2,000 procedures globally, representing a 42% increase from 2020, and initiated 10 new Senhance Surgical Programs. Four regulatory clearances were achieved, including FDA 510(k) approvals and CE Mark for the Intelligent Surgical Unit. Cash holdings reached approximately $135.8 million as of December 31, 2021. Revenue is projected between $7.9 million and $8.3 million for the year, marking a growth of 147% to 159% over the previous year.
- Over 2,000 procedures performed globally, a 42% increase from 2020.
- Ten new Senhance Surgical Programs initiated in 2021.
- Achieved four regulatory clearances, enhancing market credibility.
- Projected revenue growth of 147% to 159% year-over-year.
- Estimated fourth-quarter revenue of $2.1 - $2.5 million, indicating potential revenue fluctuations.
Fourth Quarter Highlights
-
Over 500 procedures were performed globally during the quarter, representing growth of over
25% over the fourth quarter 2020 -
Six Senhance Surgical Programs were initiated during the quarter, including two previously unannounced programs in
Germany andUkraine
Year-End Highlights
-
Over 2,000 procedures were performed globally, representing growth of over
42% compared to 2020 - In 2021, 10 Senhance Surgical Programs were initiated
-
Received four regulatory clearances:
- FDA 510(k) clearance for expansion of Machine Vision Capabilities for the Intelligent Surgical Unit™ (ISU™)
- FDA 510(k) clearance for articulating instruments
- Expanded FDA 510(k) clearance for general surgery indication
- CE Mark approval for the ISU
-
The Company had unaudited cash, cash equivalents, short-term and long-term investments, excluding restricted cash, of approximately
at$135.8 million December 31, 2021 -
Fourth quarter unaudited revenue is expected to be approximately
-$2.1 $2.5 million -
Full year 2021 unaudited revenue is expected to be approximately
-$7.9 , representing growth of$8.3 million 147% -159% over the prior year
"Digital transformation is occurring in many sectors and it’s a critical time to bring it to the OR to elevate surgery in ways that matter. Last year was a strong one for the company as we continued to empower surgeons around the globe with new tools and Clinical Intelligence for increased control, less variability, and consistently superior outcomes. Driving greater than
Market Development
2021 Senhance Program Initiations
Throughout 2021, the Company initiated 10 Senhance Surgical Program initiations: one in the US, six in EMEA, and three in
During the fourth quarter of 2021, the Company initiated six programs, one in the US, three in EMEA, and two in
Procedure Volumes
In 2021, surgeons performed over 2,000 procedures utilizing the Senhance System, representing a
Clinical Validation
During 2021, there were 21 peer-reviewed clinical papers published providing further support for the clinical utility of the Senhance System across a variety of surgical specialties. In particular, there were four milestone papers published:
- In April, a study was published comparing health economic outcomes of the Senhance System versus another robotic system, as well as traditional laparoscopy. According to the study, the Senhance System was less than half the median instrument cost compared to procedures performed on another robotic platform and was comparable to traditional laparoscopic-assisted vaginal hysterectomy costs for certain gynecologic procedures.
- In May, a study was published which analyzed the outcomes of over 800 Senhance System procedures across multiple specialties including hernia repairs, cholecystectomies, and prostatectomies based on data from the Company’s real-world clinical data registry, TRUST. According to the study, Senhance System procedures are safe and reproducible and deliver promising clinical outcomes.
- In August, a study was published which analyzed the outcomes and experience of utilizing the Senhance System to perform a high volume of urologic procedures. According to the study, the Senhance System is a safe and feasible platform to perform multiple common urologic procedures, namely upper urinary tract and extraperitoneal radical prostatectomies.
- In September, a study was published which analyzed the outcomes of inguinal hernia repair procedures based on data from the Company’s TRUST registry. According to the study, the Senhance System is a safe and doable platform to perform inguinal hernia repair procedures, and it can deliver high quality clinical outcomes related to patient recovery time, length of hospital stay, and postoperative pain.
Portfolio Expansion
Performance-Guided Surgery (PGS)
PGS builds upon the foundation of Digital Laparoscopy by adding machine vision, augmented intelligence, and deep learning capabilities to help guide improved decision making, enriched collaboration, and enhanced predictability for all surgeons, independent of training or experience, to shift the promise of consistently superior surgery into practice.
Historical advances in surgery have largely focused on bringing tools and techniques into the OR to reduce the invasiveness of procedures and improve the execution of discrete tasks. Unlike many other industries, very little focus has been on improving the decision-making aspects of the surgical process, which is crucial in the high-pressure, highly variable situations which happen repeatedly during any surgery.
PGS is the first surgical paradigm focused on a holistic solution for the entire surgeon workflow to drive consistently superior outcomes. We believe PGS can deliver real-time clinical decision support to boost surgeon capabilities to perceive complex environments, make decisions, and perform the desired tasks with increased precision, safety, and efficiency to mitigate surgical errors and complications.
Expanded Global ISU Machine Vision Capabilities
In September, the Company announced that it had received 510(k) clearance from the FDA for an expansion of machine vision capabilities on the previously cleared ISU. The ISU is utilized with the Senhance System which enables Digital Laparoscopy. The initial features of the ISU enable machine vision-driven control of the camera for a surgeon by responding to commands and recognizing certain objects and locations in the surgical field, and allow a surgeon to change the visualized field of view using the movement of their instruments. The newest ISU features expanded upon these capabilities and introduced more advanced features including: real-time 3D measurement, digital tagging, image enhancement, and enhanced camera control based on real-time data from anatomical structures while performing surgery. This is the first time any of these features will be clinically available in soft-tissue abdominal surgery.
Articulating Instrument Clearance
In July, the Company announced that it had received 510(k) clearance for 5 mm articulating instruments, which offer better access to difficult-to-reach areas of the anatomy.
General Surgery Indication Expansion
In March, the Company announced that it had received an additional FDA clearance for the Senhance Surgical System which allows for indication expansion in general surgery in the US.
CE Mark for Intelligent Surgical Unit
In January, the Company announced that it had received CE Mark approval for the ISU that enables machine vision capabilities on the Senhance System. This approval will provide Senhance Digital Laparoscopy programs in
Fourth Quarter and Full Year 2021 Revenue
For the quarter ended
Balance Sheet
As of
About
Forward-Looking Statements
This press release includes statements relating to the Senhance System and our preliminary 2021 results. These statements and other statements regarding our future plans and goals constitute "forward looking statements" within the meaning of Section 27A of the Securities Act of 1933 and Section 21E of the Securities Exchange Act of 1934, and are intended to qualify for the safe harbor from liability established by the Private Securities Litigation Reform Act of 1995. Such statements are subject to risks and uncertainties that are often difficult to predict, are beyond our control and which may cause results to differ materially from expectations and include whether we will be able to continue to progress our strategic plan in 2022; whether final 2021 fourth quarter and full year revenue will meet expectations; whether the momentum we have generated will drive accelerated adoption of the Senhance System and whether we will continue to make progress towards on the promise of Performance-Guided Surgery; whether Performance Guided Surgery can deliver real-time clinical decision support to boost surgeon capabilities to perceive complex environments, make decisions, and perform the desired tasks with increased precision, safety, and efficiency to mitigate surgical errors and complications; whether we can continue to increase Senhance System placements and sales, and whether we can continue to add foundational sites and receive regulatory clearances and approvals that we seek. For a discussion of the risks and uncertainties associated with the Company’s business, please review our filings with the
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INVESTOR CONTACT:
invest@asensus.com
or
MEDIA CONTACT:
CG Life
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