Monogram Orthopaedics Reports Full Year 2023 Financial Results
- Monogram Orthopaedics Inc. reported financial and operational results for Q4 2023.
- The company plans to accelerate 510(k) FDA submission with design modifications to reduce clinical trial risk.
- mBôs surgical robot was delivered to a global distributor, marking a revenue milestone.
- Introduced mVision technology for registration and tracking, potentially integrated into the mBôs system.
- The company aims for FDA submission in the second half of 2024 without clinical data.
- Management is confident in the modified system's equivalence arguments and safety profile.
- Monogram is fully funded for the anticipated 510(k) submission.
- 2023 was focused on product launch and pipeline development, including mVision technology.
- Future milestones include FDA clearance for mBôs, OUS clinical trial approvals, and mVision development.
- The company aims to advance orthopedic robotics with innovative solutions.
- None.
Insights
The announcement from Monogram Orthopaedics Inc. presents several key points that are likely to influence the company's market positioning and investor sentiment. The shipment of the mBôs surgical robot system to an international customer marks a significant milestone in Monogram's commercialization efforts. This event is a tangible demonstration of the company's ability to execute on its international expansion strategy. The entry into global markets can lead to diversified revenue streams and reduce dependency on domestic sales, which is a positive signal for investors looking for growth opportunities.
Furthermore, the introduction of mVision Technologies represents a strategic move to enhance the company's product offerings. This innovation could potentially disrupt the orthopedic robotics space by improving surgical outcomes and reducing operation times, which may lead to cost savings for healthcare providers. If successful, this technology could increase Monogram's competitive edge and market share, attracting interest from investors and potential strategic partners looking for novel and efficient solutions in the medical technology sector.
The 510(k) submission process is a critical regulatory pathway for medical device companies seeking to market their products in the United States. Monogram's strategy to avoid a clinical trial by making preemptive design modifications is a calculated risk that could significantly expedite the FDA clearance process. The company's proactive engagement with the FDA and the agency's understanding of the technical areas of concern are encouraging signs of a potentially smooth regulatory journey.
However, the reliance on a 510(k) submission without clinical data is contingent upon the FDA's acceptance of the company's equivalence arguments. Should the FDA require additional data, Monogram's plan to leverage overseas clinical trial results demonstrates foresight and adaptability. This dual-pathway approach to FDA clearance and international approval could mitigate the risk of regulatory delays and provide a backup plan, which is reassuring for stakeholders concerned about the uncertainties inherent in the regulatory approval process.
Monogram's financial position, as indicated by their statement of being fully funded through the anticipated 510(k) submission, offers a measure of security to investors. The ability to reach this critical regulatory milestone without the need for additional capital raises suggests prudent financial management and a lower risk of dilution for existing shareholders in the short term.
The company's mention of an aggressive strategy for OUS clinical trials and the potential for post-launch marketing or international approval also hints at a broader revenue strategy. The ability to scale operations in international markets without significant increases in selling, general and administrative (SG&A) expenses is an attractive proposition for cost-conscious investors. This approach could lead to improved profit margins and a stronger bottom line, which are key factors in assessing a company's long-term financial health and growth potential.
510(k) Submission with FDA On Track for Second Half of 2024
Shipped mBôs Surgical Robot System to First International Customer
Introduced mVision Technologies, a Novel Approach to Registration and Tracking
Management to Host Business Update Conference Call on Thursday, March 21 at 5:00 p.m. Eastern Time
AUSTIN, TX / ACCESSWIRE / March 15, 2024 / Monogram Orthopaedics Inc. (NASDAQ:MGRM) ("Monogram" or the "Company"), a medical technology company focused on reconstructive joint procedures and surgical robotics, has reported its financial and operational results for the fourth quarter and full year ended December 31, 2023.
Fourth Quarter 2023 and Subsequent Operational Highlights
- The Company's plan to aggressively accelerate 510(k) submission with design modifications that management believes reduce the risk of a clinical trial is on track. The Company anticipates Verification and Validation completion on the upgraded design as early as the first half of 2024. The Company is fully funded to anticipated 510(k) submission in the second half of 2024.
- Delivered mBôs surgical robot to one of the world's largest global robotics distributors in a first sale, representing a key revenue milestone and paving the way for broader commercialization.
- The Company is moving forward with an OUS clinical trial that will support US and OUS post-launch marketing or US 510(k) submission, depending on FDA feedback.
- Introduced mVision technology, a novel approach to registration and tracking that the company is now working on as a standalone product or for integration into the mBôs surgical robotic system in the future.
- Presented a product discussion featuring Monogram's mBôs and mVision technologies with a surgeon panel during AAOS Annual Meeting
- Presented at the Canaccord Genuity 2024 Musculoskeletal Conference
Management Commentary
"2023 was transformative for Monogram as our first year as a public company, with a focus on advancing our product launch for mBôs and the continued development of our next-gen product pipeline," said Ben Sexson, Chief Executive Officer of Monogram. "The fourth quarter was highlighted by the delivery of our first mBôs surgical robot to one of the world's largest global robotics distributors and the introduction of mVision technology.
"Throughout 2023, we were highly focused on executing our commercialization roadmap. We have employed a dynamic regulatory strategy as new facts and opportunities emerge, which supports our intention to obtain FDA clearance as expeditiously and economically as possible. We are currently in the Verification phase, with the team actively executing extensive, highly rigorous internal and external testing. We think it could be possible to complete all Verification and Validation testing as early as the first half of 2024 with a 510(k) submission without clinical data in the second half of 2024.
"We have had several formal communications with the FDA, and we believe they understand the technical areas of concern that could necessitate a clinical study. The team has preemptively made design changes related primarily to foot pedal control of the system that we believe could address the FDA's cited technical equivalence concerns and potentially obviate the need for a clinical trial. We believe the modified system has very strong equivalence arguments and a potentially favorable safety profile compared to other cleared products on the market, and the design modifications could even favorably improve the system's performance.
"This approach could potentially be quite favorable to our commercialization timeline, and based on our progress with the FDA, we believe we have sufficient funding through the 510(k) submission. We remain on target to largely complete verification and validation testing in H1 2024, a requirement for FDA submission and clearance. At the same time, we are aggressively preparing to launch OUS clinical trials with our international partners. We plan to leverage OUS clinical data to supplement our US submission should the agency require a clinical trial despite our improved equivalence profile, or for post-launch marketing in the US and international approval should the FDA clear mBôs without clinical data. We like the optionality that comes with this strategy.
"We recently announced mVision, our next-generation navigation solution designed to eliminate cart-based tracking and streamline registration and tracking to eliminate point sampling and tracking with large arrays. Our engineers plan to configure the mBôs robot to be upgradable to mVision navigation. With mVision, the goal is to minimize the risks associated with pin site fracture and infection and significantly reduce the surgical time associated with placing the arrays and registration. In addition, the goal is to minimize the surgical footprint in the OR. We are confident that mVision will advance the standard of care in orthopedic robotics.
"During the quarter, we delivered our first mBôs robot. We believe the international market for orthopedic robotics is attractive, large, and growing. The ability to scale OUS in a capital-efficient manner without the implant or significant increases to SG&A costs is also attractive. In the US, we want to own the total economics of the sale that would accrete from selling the implant, mBôs robot, and related consumables.
"Monogram's technology and its intrinsic value continue to gain recognition with surgeons in the joint reconstruction market, in which higher barriers to entry for new participants have historically reduced innovation in our view. We see an opportunity to unlock new growth within this extremely attractive market by providing a solution to the vulnerabilities in the existing economic model for robotics - namely, increased surgical time and increased consumables cost. We are confident that this fundamental value proposition will continue to garner recognition from the market and industry participants, including from potential strategic partners, as we continue to execute to generate long-term value for our shareholders.
"Looking ahead into 2024, our next milestones on the commercialization path include completing our verification and validation testing, submitting mBôs to the FDA for clearance, and obtaining approvals to run our OUS clinical trial. We will also further develop our mVision navigation technology, which could become a standalone product and/or be integrated into mBôs. Taken together, we are incredibly enthusiastic about the future for Monogram, the pace of our product timeline, and our team's ability to scale the commercialization path of our advanced, next-generation active surgical robotics," concluded Sexson.
Upcoming 2024 Milestones
- Largely complete mBôs system verification and validation - H1 2024
- Submit semi-active modality 510(k) application to FDA - H2 2024
- Commence OUS live-patient surgery trials - H2 2024
- Anticipated FDA response & expand international relationships - H2 2024
Full Year 2023 Financial Results
Research and development expenses for the year ended December 31, 2023, were
For the year ended December 31, 2023, General & Administrative expense increased to
Net loss was
Cash and cash equivalents totaled
Business Update Conference Call
Monogram Chief Executive Officer Ben Sexson, Chief Medical Officer Doug Unis, MD, Chief Technology Officer Kamran Shamaei, and Chief Financial Officer Noel Knape will host the conference call, followed by a question-and-answer period.
To access the call, please use the following information:
| Date: | Thursday, March 21, 2024 |
| Time: | 5:00 p.m. Eastern time (2:00 p.m. Pacific time) |
| Registration Link: | https://streamyard.com/watch/Cqvuk6Z3nsUg |
A replay will be available after the call and will be available in the Company's investor relations section here.
About Monogram Orthopaedics
Monogram Orthopaedics (NASDAQ: MGRM) is working to develop a product solution architecture with the long-term goal of enabling patient-optimized orthopedic implants at scale by linking 3D printing and robotics with advanced pre-operative imaging. The Company has a robotic system that can autonomously execute optimized paths for high-precision insertion of implants in synthetic bone specimens. Monogram intends to produce and market robotic surgical equipment and related software, orthopedic implants, tissue ablation tools, navigation consumables, and other miscellaneous instrumentation necessary for reconstructive joint replacement procedures. The Company has not yet made 510(k) premarket notification submissions or obtained 510(k) clearances for its robotic products. FDA approval is required to market these products, and the Company has not obtained FDA approval for any of its robotic products, and it cannot estimate the timing or assure the ability, to obtain such clearances.
Monogram Orthopaedics is working to advance the way orthopedic surgery is done. Our system is being developed to combine personalized knee implants with precision robotic surgical assistants to hopefully give patients a better-fitting knee replacement with minimally invasive surgery. One hundred thousand knee replacements failing each year in a
To learn more, visit www.monogramorthopedics.com.
Forward-Looking Statements
This press release may include "forward-looking statements.'' To the extent that the information presented in this presentation discusses financial projections, information, or expectations about Monogram Orthopaedics Inc.'s business plans, results of operations, products or markets, or otherwise makes statements about future events, such statements are forward-looking. Such forward-looking statements can be identified by the use of words such as "should," "may," "intends," "anticipates," "believes," "estimates," "projects," "forecasts," "expects," "plans," and "proposes."
Although Monogram Orthopaedics Inc. believes that the expectations reflected in these forward-looking statements are based on reasonable assumptions, there are a number of risks and uncertainties that could cause actual results to differ materially from such forward-looking statements. You are urged to carefully review and consider any cautionary statements and other disclosures, including the statements made under the heading "Risk Factors" and elsewhere in the offering statement filed with the SEC. Forward-looking statements speak only as of the date of the document in which they are contained, and Monogram Orthopaedics Inc. does not undertake any duty to update any forward-looking statements except as may be required by law.
Investor Relations
Chris Tyson
Executive Vice President
MZ North America
Direct: 949-491-8235
MGRM@mzgroup.us
MONOGRAM ORTHOPAEDICS INC.
BALANCE SHEETS
December 31, 2023 | December 31, 2022 | |||||||
Assets | ||||||||
Current assets: | ||||||||
Cash and cash equivalents | $ | 13,589,028 | $ | 10,468,645 | ||||
Account receivable | 364,999 | - | ||||||
Prepaid expenses and other current assets | 664,262 | 788,004 | ||||||
Total current assets | 14,618,289 | 11,256,650 | ||||||
Equipment, net | 945,020 | 1,082,442 | ||||||
Intangible assets, net | 548,750 | 758,750 | ||||||
Operating lease right-of-use assets | 466,949 | 592,221 | ||||||
Total assets | $ | 16,579,008 | $ | 13,690,063 | ||||
Liabilities and Stockholders' Equity | ||||||||
Current liabilities: | ||||||||
Accounts payable | $ | 2,462,268 | $ | 663,170 | ||||
Accrued liabilities | 227,684 | 748,460 | ||||||
Warrant liability | - | 7,519,101 | ||||||
Operating lease liabilities, current | 128,266 | 118,166 | ||||||
Total current liabilities | 2,818,218 | 9,048,897 | ||||||
Operating lease liabilities, non-current | 363,724 | 491,989 | ||||||
Total liabilities | 3,181,942 | 9,540,886 | ||||||
Commitments and contingencies | - | - | ||||||
Stockholders' equity: | ||||||||
Series A Preferred Stock, $.001 par value; 0 and | - | 4,898 | ||||||
4,897,553 shares issued and outstanding at December | ||||||||
Series B Preferred Stock, $.001 par value; 0 | - | 3,196 | ||||||
and 3,195,667 shares issued and outstanding at December | ||||||||
Series C Preferred Stock, $.001 par value; 0 and 438,367 | - | 438 | ||||||
shares issued and outstanding at December 31, 2023 | ||||||||
Common stock, $.001 par value; 90,000,000 shares | 31,338 | 9,674 | ||||||
authorized, 31,338,391 and 9,673,870 shares issued | ||||||||
Additional paid-in capital | 64,874,392 | 41,894,417 | ||||||
Accumulated deficit | (51,508,664 | ) | (37,763,447 | ) | ||||
Total stockholders' equity | 13,397,066 | 4,149,176 | ||||||
Total liabilities and stockholders' equity | $ | 16,579,008 | $ | 13,690,063 | ||||
MONOGRAM ORTHOPAEDICS INC.
STATEMENTS OF OPERATIONS
| Years Ended | ||||||||
December 31, 2023 | December 31, 2022 | |||||||
Revenue | $ | 364,999 | $ | - | ||||
Operating expenses: | ||||||||
Research and development | 10,585,884 | 5,384,710 | ||||||
Marketing and advertising | 2,994,389 | 2,743,687 | ||||||
General and administrative | 4,052,755 | 2,484,750 | ||||||
Total operating expenses | 17,633,028 | 10,613,147 | ||||||
Loss from operations | (17,268,029 | ) | (10,613,147 | ) | ||||
Other income (expense): | ||||||||
Grant income | - | 256,000 | ||||||
Change in fair value of warrant liability | 3,088,533 | (3,431,865 | ) | |||||
Interest income and other, net | 434,279 | 98,065 | ||||||
Total other income (expense) | 3,522,812 | (3,077,800 | ) | |||||
Net loss before taxes | (13,745,217 | ) | (13,690,947 | ) | ||||
Income taxes | - | - | ||||||
Net loss | $ | (13,745,217 | ) | $ | (13,690,947 | ) | ||
Basic and diluted loss per common share | $ | (0.61 | ) | $ | (1.42 | ) | ||
Weighted-average number of basic and diluted shares outstanding | 22,409,222 | 9,673,870 | ||||||
MONOGRAM ORTHOPAEDICS INC.
STATEMENTS OF CASH FLOWS
| Years Ended | ||||||||
| December 31, 2023 | December 31, 2022 | |||||||
Operating activities: | ||||||||
Net loss | $ | (13,745,217 | ) | $ | (13,690,947 | ) | ||
Adjustments to reconcile net loss to net cash used in operating activities: | ||||||||
Stock-based compensation | 1,558,779 | 743,274 | ||||||
Other expenses settled with stock issuances | 130,000 | - | ||||||
Loss from change in fair value of common stock make-whole obligation | 44,333 | - | ||||||
Depreciation and amortization | 412,335 | 386,686 | ||||||
Change in fair value of warrant liability | (3,088,533 | ) | 3,431,865 | |||||
Changes in non-cash working capital balances: | ||||||||
Account receivable | (364,999 | ) | - | |||||
Prepaid expenses and other current assets | 269,697 | 189,906 | ||||||
Accounts payable | 1,799,098 | 214,138 | ||||||
Accrued liabilities | (565,109 | ) | 283,983 | |||||
Operating lease assets and liabilities, net | 7,107 | 21,543 | ||||||
Cash used in operating activities | (13,542,509 | ) | (8,419,553 | ) | ||||
Investing activities: | ||||||||
Purchases of equipment | (64,913 | ) | (241,203 | ) | ||||
Cash used in investing activities | (64,913 | ) | (241,203 | ) | ||||
Financing activities: | ||||||||
Proceeds from issuances of Common Stock, net | 15,330,763 | - | ||||||
Proceeds from issuances of Series B Preferred Stock, net | - | 9,615,078 | ||||||
Proceeds from issuances of Series C Preferred Stock, net | 147,042 | 3,978,613 | ||||||
Proceeds from warrant exercise | 1,250,000 | - | ||||||
Cash provided by financing activities | 16,727,805 | 13,593,691 | ||||||
Increase in cash and cash equivalents during the year | 3,120,383 | 4,932,935 | ||||||
Cash and cash equivalents, beginning of the year | 10,468,645 | 5,535,710 | ||||||
Cash and cash equivalents, end of the year | $ | 13,589,028 | $ | 10,468,645 | ||||
Cash paid for interest | $ | - | $ | - | ||||
Cash paid for income taxes | $ | - | $ | - | ||||
Non-cash investing and financing activities: | ||||||||
Increase in right of use asset and lease liability from new lease agreement | $ | - | $ | 308,474 | ||||
Issuance costs related to Common Stock Purchase Agreement settled through issuance of Common Stock | $ | 247,980 | $ | - | ||||
Cashless exercise of warrant | $ | 926,335 | $ | - | ||||
SOURCE: MONOGRAM ORTHOPAEDICS INC
View the original press release on accesswire.com
FAQ
When is Monogram Orthopaedics Inc. planning to submit a 510(k) to the FDA?
What is the significance of delivering the mBôs surgical robot to a global distributor?
What is mVision technology introduced by Monogram Orthopaedics Inc.?
What are the future milestones mentioned by Monogram Orthopaedics Inc. for 2024?
Who is the Chief Executive Officer of Monogram Orthopaedics Inc.?
