Thanks, operator, and welcome everyone to our first quarter 2023 earnings call. I am joined on today's call by our Chief Financial Officer, Tara Semb. Let me provide you with a brief outline of what we intend to cover today. I'll begin with the review of our revenue results and the factors that contributed to our sales performance in the first quarter. I'll then share an update on our operational progress made during the first quarter and in recent weeks. Tara will discuss our first quarter financial results in detail as well as our financial guidance for 2023, which we updated in our earnings release today. I'll then conclude with some additional thoughts on our outlook and strategic priorities for the remainder of 2023, before we open the call with questions. With that, let's begin with the review of our Q1 revenue results. In the first quarter, our total revenue decreased 3% year-over-year to $12.1 million, exceeding the high-end of our expectations that we shared on our fourth quarter earnings call by approximately $900,000. Our stronger than anticipated total revenue performance was largely driven by Advanced Energy sales, which decreased 10% year-over-year to $9.7 million, exceeding the high-end of our expectations by approximately $700,000. OEM sales increased 46% year-over-year to $2.5 million and approximately $200,000 higher than we had anticipated. Looking ahead at our Advanced -- looking at our Advanced Energy sales performance in more detail, as anticipated during the first quarter, we continue to experience disruption in global sales of our Advanced Energy products due to the medical device safety communication that was posted by the FDA in March of 2022. The 10% decrease in sales in our Advanced Energy products was driven by global sales of generators and handpieces, which both decreased by more than 10% year-over-year. While the year-over-year decrease in global handpiece sales was largely consistent with the trends observed in the fourth quarter of 2022, we were pleased to see notable improvement in global generator sales trends in Q1. While global generator revenue declined year-over-year, the trends improved materially when compared to the nearly 50% year-over-year decline in generator sales reported in Q4. In terms of our Advanced Energy performance in the U.S., we were pleased to see sales of our Advanced Energy products in the U.S. increase by nearly 10% year-over-year with sales of our U.S. generators increasing by approximately 40% year-over-year. Our generator sales performance in the U.S. benefited from the introduction of our Apyx One Console, our next-generation generator, which we launched in late January. In connection with the launch, we introduced an upgrade program for all of our existing U.S. users enabling them to trade in their prior version of our Renuvion Generator and receive our Apyx One Console at a discounted rate. We were pleased with the initial demand we have seen from our existing users, which exceeded our expectations in the quarter, and drove the majority of our outperformance that we saw versus our expectations. While sales of our generators to new customers continued to remain paced by the confusion related to the safety communication, we were also pleased with the initial sales of our Apyx One Console to new customers as well, which modestly exceeded our expectations. With respect to our Advanced Energy sales outside the U.S., international generator sales decreased by more than 60% year-over-year, which was modestly below what our guidance range had assumed for Q1. Advanced Energy generator sales in all markets continued to be impacted by the safety communication with weaker demand from distributors in key countries most notably Europe and the Asia-Pacific region. Our international sales results were moderated somewhat by more modest declines in sales of our handpieces. In summary, despite the continued headwinds related from the safety communication, which were largely consistent with our expectations for the first quarter, we were pleased to drive stronger than anticipated sales of our Apyx One Console both to existing and new U.S. customers. This helped to partially offset the impact of disruption as regulatory and clinical teams continue to work to address the remaining limitations of the safety communication. Shifting to a discussion of our operational performance. During the first quarter, we were pleased to achieve strong progress with respect to our regulatory strategy while raising awareness of our recently obtained clinical indications, including our next-generation generator and securing additional capital to strengthen our balance sheet. Let me discuss each of these in turn beginning with our regulatory strategy. During the first quarter, our regulatory and clinical teams remain focused on securing FDA 510(k) clearances for specific clinical indications to expand our ability to market and sell our Renuvion technology and address the remaining limitations of the safety communication. Following our submission of a 510(k) application at the end of 2022, we were pleased to receive clearance in late February for a new clinical indication related to the use of our Renuvion APR handpiece for the contraction of soft tissue including subcutaneous tissue where needed. This clearance provides important support for our safety and effectiveness of Renuvion when used for this purpose anywhere on the body. We also completed and submitted our request for additional 510(k) clearance to obtain an indication for the coagulation of subcutaneous soft tissues following liposuction for aesthetic body contouring. Our 510(k) submission was supported by a comprehensive portfolio of clinical and real world evidence demonstrating the safety and efficacy of our Renuvion APR handpiece when used following liposuction procedures, which included data from our IDE clinical study in skin laxity and treatment data from more than 480 patients in 1,180 areas of the body. As a reminder, an analysis we conducted comparing this data to real world evidence for liposuction treatments gathered in a literature review showed that the use of Renuvion procedures following liposuction procedures demonstrated no new or increased risk when compared to liposuction procedures alone. With this as a backdrop, on April 28, we were very excited to announce that we received clearance for this indication. With the receipt of this 510(k) clearance, the Renuvion APR handpiece is now the only device on the market with a 510(k) clearance for use following liposuction. As we have stated previously, we believe this indication directly addresses the remaining limitations of the safety communication as last updated on July 21, 2022, specifically the language stating that the Renuvion APR handpiece has not been cleared for the use in combination with liposuction and advising against the use of our technology in combination with liposuction. To that end, we were pleased to receive confirmation that the FDA posted an update to the safety communication on May 10, 2023. This update was intended to inform consumers and healthcare providers about the clearance of the Renuvion APR handpiece for use under the skin in certain procedures intended to improve the appearance of skin, including for coagulation of subcutaneous soft tissues following liposuction for aesthetic body contouring. The update included revised recommendations for consumers as well as revised recommendation for healthcare providers, the latter of which highlighted three new specific indications for our Renuvion APR handpiece, including for soft tissue contraction where needed following liposuction for aesthetic body contouring and for dermatological and aesthetics procedures to improve the appearance of lax skin. They also highlighted the new specific indication for our Renuvion dermal handpiece for treatment of moderate to severe wrinkles and rhytides. Importantly, the updated safety communication also included the FDA's intention to continue to monitor reports of adverse events for other minimally invasive soft tissue heating devices in aesthetic skin procedures and work to ensure that consumers and healthcare providers are informed about the intended uses of these devices. We believe that the May 10, 2023, FDA update to the safety communication addresses the issue set forth in the original safety communication from March 14, 2022. I am extremely proud of the hard work and dedication to our strategy from our clinical and regulatory teams in the time since the safety communication was posted in March of 2022. Without their efforts, the significant progress we have made since that time would not have been possible. In addition to our recent regulatory progress, we continue to raise awareness of the two specific clinical indications that we obtained in 2022 for the root use of our Renuvion technology in dermatological procedures for the treatment of moderate to severe wrinkles and rhytides and to improve the appearance of lax or loose skin in the neck and the submental region. We commenced the U.S. commercial launch for these indications at the beginning of January, which was accompanied by This is Me, our first direct-to-consumer brand campaign. This is Me is a nationwide integrated brand campaign that includes a new patient focused website, brochures, and online videos, new social media content, and digital advertising across multiple platforms. The overarching goal of this campaign is to grow the awareness of our technology and its potential to help people achieve the results they are looking for through a minimally invasive procedure while preserving the defining physical features that make them who they are. In addition to the response and feedback we have received from our surgeons and patients, we continue to be -- which continue to be very positive, our integrated campaign has generated millions of impressions to-date, and we have seen an increase in our total social media engagement. We have also continued to see new mentions of our technology across various media outlets, including magazines like Marie Claire and NewBeauty and on TV, a procedure with Renuvion to correct a patient's sagging neck was recently demonstrated in a February episode of the Lifetime series -- channel series, The Balancing Act that included an interview between show host Montel Williams and the performing surgeon to discuss the procedure. Although, we remain in the initial months of our campaign and launch, we have been very pleased with the response we have seen so far. Turning to an update of our new product innovation. At the end of January, we were pleased to begin the U.S. commercial launch of the Apyx One Console. As a reminder, this next-generation version of our Renuvion generator was redesigned to enhance its functionality and ease of use and improve the overall user experience for our surgeon customers. Its enhanced features include touchscreens featuring new and intuitive user interface presets for specific procedures in areas of the body, an advanced gas system that measures and monitors gas volume and usage, and new cloud connectivity features including the ability to log and share data, install updates, and troubleshoot the device remotely. The Apyx One design and features were developed in collaboration with a team of surgeons and informed by feedback of our customers. We believe the benefits of this user centric approach to product development are reflected in the positive initial feedback we have garnered from both new and existing users of our technology. As I mentioned earlier, we have been pleased with the initial market response to our Apyx One Console from a commercial standpoint as well, which contributed to our stronger than anticipated sales performance in the first quarter. Based on the promising initial response we have seen, we look forward to drive the adoption of our new generator system to both new and existing surgeon customers as we progress through 2023. During the first quarter, we were also pleased to see new clinical and academic publications discussing the use of our Renuvion technology in cosmetic surgery procedures. In January, our technology was featured in multiple chapters of a new textbook focused on body contouring procedures titled the Manual of Cosmetic Surgery and Medicine. The publication features a chapter dedicated to the use of our technology in body contouring and the use of our technology in combination with liposuction is referenced in additional chapters. We were pleased to see Renuvion described as one of the best technologies to-date in skin tightening. And on March 8, we saw a new clinical article published in the peer-reviewed Aesthetic Surgery Journal. The article summarized the methodology and the results of our multi-site IDE clinical trial to evaluate the use of Renuvion to improve the appearance of loose skin in the neck and submental region and was authored by the investigators that conducted the trial. These are just a few recent examples of the growth we continue to see in the body of clinical and academic support for our technology. Lastly, we completed our sales performance and operational progress during the first quarter by completing multiple initiatives to improve our operating efficiency and secure additional capital to further strengthen our balance sheet. In January, we implemented a series of measures to better align our operating expenses with our anticipated needs and priorities. These measures included the consolidation of our handpiece assembly lines in Clearwater, Florida manufacturing facility, which we believe will enable us to reduce our expenses in 2023 without impacting our ability to serve our current and future customers. In February, we entered into a new five-year agreement with MidCap Financial for a credit facility of up to $35 million consisting of a revolver and a term loan, which provided us with approximately $8.1 million of net proceeds at closing. Subsequent to quarter end, on May 8, we completed our previously announced sale and leaseback transaction for our Clearwater property providing us with approximately $6.6 million in proceeds net of commissions, expenses, taxes, first month's rent and expense fees, and a security deposit equal to one year's rent expense. And we are still waiting to receive the cash tax refunds of at least $7.5 million from the IRS, which were approved by the IRS in January. Stepping back with more than $16 million of cash on our balance sheet at quarter end along with the $6.6 million of net proceeds received via our recent sale and leaseback transaction, our anticipated cash refunds, and the potential capacity under our credit agreement, we continue to believe we have ample liquidity to support our near-term operations and growth initiatives. In tandem, we remain focused on driving progress to achieve our longer-term goals of sustainable profitability and strong free cash flow generation. With that, let me turn it over to Tara to review our first quarter financial results and 2023 guidance, which we updated in today's press release. Tara?