Thank you, Jonathan. Good afternoon and thank you for joining us for CONMED's Second Quarter 2023 Earnings Call. With me on the call is Todd Garner, Executive Vice President and Chief Financial Officer. Our plan is to share with you our second quarter results and then open the call to your questions. I will start by saying we are incredibly pleased with our team's performance in the second quarter. After setting a new quarterly sales record in Q1, we handily beat that with our Q2 performance. Total sales for the quarter were $317.7 million, representing a year-over-year increase of 14.6% as reported and an increase of 16.6% in constant currency. On an organic constant currency basis, sales growth finished at 12.6%. Our commercial teams were outstanding in the first half and the results in orthopedics and general surgery indicate we delivered balanced growth across our product offering on a global basis. I'd remind everyone that in mid-June, the In2Bones business reached its one-year anniversary. We remain pleased with this business and look forward to continued growth in this exciting market as part of our organic base. Additionally, the BioBrace offering continues to build momentum through growing market acceptance, which is being driven by positive clinical experiences. From an earnings perspective, during the second quarter, our GAAP net income totaled $13.7 million. This compares to a net loss of $168.3 million in the second quarter of 2022 due primarily to the extinguishment of most of the 2024 convertible notes. Excluding special items that affected comparability, our adjusted net income of $26.1 million increased 5.3% year-over-year and our adjusted diluted net earnings per share of $0.83 increased 9.2% year-over-year. At a macro level and consistent with my first quarter comments, the underlying surgical markets that we serve are healthy and health care staffing levels continue to improve. Conversely, inflationary pressure on the material side has been slower to dissipate and supply chains are not yet fully recovered. Overall, we see all these dynamics as stable to improving in the second half of 2023. In summary, I'm very pleased with the focus and results delivered in the quarter, and I'm confident we will build on our success in the second half. Before I turn the call over to Todd, I'd like to provide important context about the standard insufflation market and our competitive position with AirSeal. Let me start by saying that AirSeal is an only-in-class technology. From day one, it has been replacing standard insufflation from all marketplace competitors in both robotic and laparoscopic procedures given its unmatched clinical benefit delivered through low pressure. The introduction of another standard insufflation device into the market will not change our clinical or sales algorithm, whether it is it a stand-alone device or attached to a robot. The only parties that will feel the pressure from the introduction of another standard inflation device are the existing standard insufflation companies that we have been replacing for the past seven years. I will again remind you that none of these companies can deliver consistent pneumo at low pressure nor the related clinical benefits which are significant and are included in the investor presentation that we posted this afternoon. Our position has always been that AirSeal delivers better patient outcomes and competitive devices, driven principally through lower pressure. To support that position, we have 33 peer-reviewed studies with over 6,000 enrolled patients across five surgical specialties that demonstrate reduced postoperative pain, reduced length of stay, reduced 30-day visits, reduced ER visits, and improved ventilation metrics. Standard insufflation has zero clinical studies that demonstrate any of these important clinical benefits. In fact, I think I can make a compelling argument that we are, through our clinical capabilities, growing the number of available surgeries that can be done laparoscopically in certain patient populations to include elevated risk and high body mass index patients. Competitively, since 2018, six new insufflation devices have been introduced to the market and AirSeal continues to win surgeons globally. While the concept of integration of advice with a robot may enhance ease of use, it will do nothing to change the clinical paradigm on which we have been taking market share, and we'll continue to take market share. I will also remind you that in 2018, two strong competitors introduced their AirSeal equivalents, and I think our results would suggest we navigated that period just fine. From a technology and sustainability standpoint, we own 187 issued patents and have another 124 pending. They extend our patent position through the end of the 2030s and we continue to add to this position. Further, our AirSeal IP crosses the system and is integrated in such a way that is not one seminal patent that protects us, but rather the integration of the patents across all aspects of the system to include the IFS box, tube set and access ports. This is what makes AirSeal function in a manner that delivers clinical benefit. Each of these components is manufactured separately in a unique facility with the critical parts being in-sourced here at CONMED. We're not currently aware of any patent work that will allow another device to function in a low-pressure mode. Finally, based on the June 2023 best hospitals in the US teaching hospital category, AirSeal is present in 92% of the top 25 teaching institutions with MIS procedural utilization rates ranging from just getting started to over 75%. This is a statistically significant fact given that physicians utilize what they are trained on when they depart to surgical practice. We will never be dismissive of competitive entrants, but I think it's misinformed to assume that same old technology created by the same partner to the rest of the insufflation market will somehow materially impact our results. Never mind that the market knows minimal details about this device. From my chair, if it's not obvious that it can provide consistent pneumoperitoneum at low pressure as proven through clinical studies like AirSeal has shown, it is just another standard insufflation device. The only in-class AirSeal technology supported by extensive clinical benefits derived through low pressure has clearly been moving the market to embrace our solution. We do not see anything in a standard insufflation offering that would slow that progression, and we remain extremely optimistic about our future with AirSeal. More importantly, and if you really digest the quarter we just delivered, the overall prospects for CONMED, given the surgical diversity of and balanced growth our portfolio is demonstrating look the best they have ever looked in my tenure. I'll now turn the call over to Todd, who will provide further details on our financial performance and discuss our updated outlook. Todd?