Robert Ball
Analyst · Goldman Sachs
Thanks, Sam. Good afternoon, everyone, and welcome to our first quarter earnings call. I'm very pleased to report that 2026 is off to a strong start. Through the first few months of the year, we've rapidly onboarded new surgeons, deepened utilization within our existing customer base and achieved several important product milestones. This performance reflects intensifying momentum across our entire organization, which enabled us to deliver first quarter net revenue of $16.7 million, an increase of 65% year-over-year and 16% sequentially. First quarter gross margin also came in strong at 77.7%. And we see further opportunity for expansion as the organization continues to mature. Given the strength of these results, our growing scale and the efficiency of our commercial organization more broadly, we've increased conviction in the trajectory of our business. And as a result, we are raising our full year 2026 net revenue guidance today to a range of $65 million to $68 million, representing growth of 37% to 44% over 2025. This compares to our prior range of $62 million to $65 million or 31% to 37% growth. Jeff will provide additional color on our outlook shortly. Our ability to deliver this growth in 2026 is grounded in the same 3 strategic priorities we discussed on our last 2 calls, which include driving adoption among new surgeons, increasing penetration in our existing surgeon customer base to increase procedural volume, and adding products to our portfolio to address the remaining unmet needs of patients and surgeons. This includes both expanding indications and enabling technology. We've made meaningful progress on all 3 priorities in the first quarter, which I'll walk through now. Let me start with new surgeon adoption. Our W-2 commercial leadership organization remains laser-focused on the roughly 1,800 high-volume shoulder specialists in the U.S. And that targeted approach continues to translate into rapid growth in our customer base of core and contender surgeon customers. We are very pleased with the new surgeon adoption trends we're seeing through the early part of 2026. And we expect that momentum to be durable throughout the year. As a reminder, we ended 2025 with 134 core and contender surgeons, up 61% year-over-year and we'll update that figure on an annual cadence. Surgeon adoption continues to be driven by focused execution from our commercial leadership team, supported by our proprietary business intelligence platform. We are increasingly seeing the brand awareness we've built in the market over the past year compound that effort. Finally, we're benefiting from the accelerating productivity gains within the W-2 commercial leadership cohort hired in 2025. To capitalize on this growing momentum, we again added top talent to our commercial leadership team through Q1 to support further scaling of our business, particularly as we secure additional hospital approvals in key new territories. We are making progress with activating these markets and believe there is significant greenfield opportunity remaining across the U.S. for our team to target. We look forward to the contributions from these new commercial leaders as they ramp over the next couple of quarters and build deeper relationships within their territories. Meanwhile, we've continued to invest in terms of new surgeon adoption coming out of these sessions and increasingly view them as an integral part of our broader commercial strategy. Excluding industry meetings, our CEME team conducted 44 total SI-sponsored educational events in first quarter. And the peer-to-peer dynamic these events create generates organic advocacy that compounds across the Shoulder surgical community. Most recently, in April, we hosted our first National Symposium of 2026 in Napa Valley. Surgeon attendance was up over 70% versus last year's event, making it the largest symposium in SI's history since we launched the program 4 years ago. These symposiums combine digastric content, case-based discussion and hands-on experience with our InSet Shoulder arthroplasty portfolio and ProVoyance's preoperative planning platform with curriculum designed, written and proctored all by surgeons. The consistent positive feedback we received from attendees at these events validates the incredible work of our CEME team in creating a true differentiator in the marketplace that's generating tangible results, both in terms of generating interest among new surgeons and helping to drive our second key strategic priority of increasing utilization and procedural growth within our customer base. For example, of the attending surgeons at our NAPA course who are not already core or contender customers, more than 70% have already either performed their first case with our system, committed to their first case or committed to increasing volume. And that progression has occurred in just a few weeks since the meeting. When looking at the first quarter specifically, total implant volume across our core contender and prospect customers increased 51% year-over-year to 2,184 units. As has been the case in recent quarters, this volume growth reflected a combination of several additional compelling dynamics. First, surgeons are entering our new customer funnel faster. In fact, in the first quarter, we more than doubled the number of new customers entering our funnel as compared to the first quarter of 2025. Second, surgeons are scaling through the funnel from prospect to contender to core at a faster pace. And third, we're seeing increased volume from existing surgeons within their current prospect contender and core categories. Within these dynamics, the standout signal is that our highest growth surgeon category in the first quarter was core, both year-over-year and sequentially, which is the strongest possible signal of where our business is heading. The one category where growth has moderated is contender. And that's by design because we are losing those contenders to core status. Importantly, even as we rapidly added core surgeons, we've continued to see increases in units per surgeon, both year-over-year and sequentially in that category. This is particularly meaningful proof point. New entrants to the core category typically join at the lower end of the volume range, which would normally compress the average. But our highest volume core surgeons more than offset that dynamic, demonstrating that our existing core surgeons are continuing to grow their utilization even as the segment expands. To ensure we continually equip these surgeons and best-in-class product portfolio, we've also remained focused on our third strategic priority of developing and launching new technologies to address the remaining unmet needs of patients and surgeons, both through new indications and enabling technology. We've had an active few months on this front to start the year. And I want to highlight a couple of specific areas of progress. Starting with new indications. Consistent with our prior communicated timing, we initiated a limited user release of our I-135RFX products in early Q1. We recently expanded the indication to include more complex fractures. And 2 weeks ago, we announced the transition of our InSet 135RFX Humeral Stem from limited user release to full commercial launch following receipt of that expanded clearance from FDA. With this broader label, the I-135 now addresses primary revision and fracture total shoulder arthroplasty cases and equally important, its addition to our portfolio means that Shoulder Innovations can now nearly support the I-135 joins the smaller form factor I-195 and I-70 launched in 2024 and 2025, respectively, as the third addition to the I-Series humeral stem product line. Consistent with those earlier launches, the I-135 is built on our exclusive InSet lateral-lateral implant philosophy, which independent peer-reviewed research has shown reduces complications and maximizes postoperative range emotion. To date, surgeons have used the I-135 in both anatomic and reverse shoulder arthroplasty configurations and consistent feedback has highlighted its ease of use, straightforward surgical technique and seamless integration with our 2 tray surgical instrumentation system. Underpinning the clinical confidence behind the 135 and our entire implant portfolio is the real-world evidence we're building to our clinical data registry. We've now enrolled over 500 patients across both anatomic and reverse shoulder arthroplasty configurations. And we continue to believe this registry will generate a robust body of evidence that strengthens our position with surgeons, health systems and patients over time. Separately on the new product front, we initiated a limited user release of our N22 Glenosphere in the first quarter and have been pleased with this reception associated with allergic reactions for metal implants. We view this as an exciting incremental addressable market and look forward to providing further updates on our full launch plans in the months ahead. Turning now to enabling technology. Since announcing in December, our strategic partnership with Interventional Systems to introduce a shoulder-specific micro-robotic solution for shoulder arthroplasty. We've made tangible progress with respect to product development and remain incredibly excited with the mid- and longer-term economic and competitive opportunities associated with this technology. As a reminder, the solution is designed to integrate directly with our ProVoyance platform to deliver a seamless enabling technology experience from preoperative planning through intraoperative execution, allowing surgeons to plan in ProVoyance and deploy that plan in the operating room as a single connected workflow. In March, we performed yet another cadaver lab, which further reinforced our conviction that Interventional Systems' technology is indeed the right product for this robotic application in shoulder arthroplasty. This particular cadaveric session encompass the entire procedure, beginning with the CT scan through ProVoyance through operating the robot, placing the device in a cadaveric specimen as intended. Product development for the robotic solution is progressively slightly ahead of schedule. We are targeting 510(k) submission in 2027. We look forward to sharing additional updates regarding timing and product features on our future earnings call this year. As a final note and stepping back across everything we've discussed today, we are increasingly finding that focused shoulder-specific nature of our ecosystem is attracting interest from partners who see the value in reaching this market through us. And that excitement is only growing as we scale, whether through programs like our robotic development initiative or best-in-class implant portfolio or the strong clinical outcome surgeons are achieving with our products. As we look ahead, we are excited about a number of near-term opportunities we see to further expand the breadth of our Shoulder solutions we offer surgeons and patients, both through our own innovative vision through the relationships that market leadership attracts. We look forward to sharing more updates on these opportunities in coming quarters. With that, I'll now turn the call over to Jeff to review our first quarter results in more detail and provide an update on our outlook for 2026.