Hello, and thank you for standing by. Welcome to Aziyo Biologics, Fourth Quarter and Full Year 2021 Earnings Conference Call. At this time, all participants are in a listen-only mode. After the speaker’s presentation, there will be a question-and-answer session. [Operator Instructions]. I would now like to hand the conference over to Leigh Salvo with Investor Relations. Please go ahead.

Thank you. And thank you all for participating in today's call. Joining me are Ronald Lloyd, Chief Executive Officer, and Matthew Ferguson, Chief Financial Officer. Earlier today, Aziyo released financial results for the quarter and full year ended December 31st, 2021. A copy of the press release is available on the company's website. Before we begin, I'd like to remind you that management will make statements during this call that include forward-looking statements within the meaning of federal securities laws, which are made pursuant to the Safe Harbor provision of the Private Securities Litigation Reform Act of 1995. Any statements contained in this call that do not relate to matters of historical fact or relate to expectations or predictions of future events, results, or performance are forward-looking statements. All forward-looking statements, including without limitation, those relating to our operating trends and future financial performance, the impact of COVID-19 on our business and prospects for recovery, expense management, expectations for hiring, growth in our organization, market opportunity, guidance for revenue, gross margin, and operating expenses, commercial expansion and product pipeline development, expected future product launches and milestones and expected results and performance of our partnership and commercial products, including patient outcomes, are based upon our current estimates and various assumptions. These statements involve material risks and uncertainties that could cause actual results or events to materially differ from those anticipated or implied by these forward-looking statements. Accordingly, you should not place undue reliance on these statements. For listening description of the risks and uncertainties associated with our business based upon to the Risk Factors section of our public filings with the SEC, including Aziyo's quarterly report on Form 10-Q for the quarterly period ended September 30, 2021. As such factors may be updated from time to time in Aziyo's other filings with the SEC, including Aziyo's annual report on Form 10-K for the fiscal year ended December 31, 2021, to be filed with the SEC accessible on the SEC website at www.sec.gov. This conference call contains time sensitive information and is accurate only as of the live broadcast today March 3, 2022. Aziyo Biologics disclaims any intention or obligation except as required by law to update or revise any financial projections or forward-looking statements, whether because of new information, future events, or otherwise. Also, during this presentation, we refer to gross margin excluding intangible asset amortization, which is a non-GAAP financial measure. A reconciliation of this non-GAAP financial measure to the most directly comparable GAAP financial measure is available on the company's earnings release for the fourth, fifth quarter at its full year ended December 31, 2021. Which is accessible on the SEC's website and posted on the Investor page of Aziyo's website at www.aziyo.com. And with that, I'll turn the call over to Ronald.

Thanks, Leigh. Good afternoon, and thank you all for joining us. I'm incredibly proud of the progress we've made in setting up 2022 as a breakout year for Aziyo. By the end of this month, we anticipate submission of a form 10-K application for CanGaroo RM, our next-generation envelope, and continue to plan for this product launch in the second half of the year. Targeting an estimated $600 million annual addressable market, we believe CanGaroo RM has a potential reach more than $100 million in annual revenues and be a core driver of our value creation over the next several years. In parallel, we've continued to advance SimpliDerm, our soft tissue reconstruction product, as well as our orthopedic and spine repair platform through a combination of product development, clinical data that expanded market access, and new distribution partnerships. These products not only contribute to our top-line revenue today, but are additional drivers of future growth. In December, we completed a pipe financing that yielded net proceeds of approximately $13.8 million, which enables Aziyo to further scale our commercial activities, generate data through ongoing clinical studies and support the remaining development costs associated with the filing for CanGaroo RM. As we reflect on 2021, undoubtedly our team navigated through unprecedented challenges, both from the enduring disruptions associated with the pandemic, as well as the FiberCel related recall. Despite these extraordinary headwinds, the goals and timelines that we've been working towards since our decision to become a publicly traded company in 2020, have remained largely on track. I am confident we have the right levers in place to ensure Aziyo success and deliver long-term value to our customers and shareholders. With that as a backdrop, I'll now provide highlights and updates for each of our product portfolios. Starting with our flagship product,…

Thanks, Ronald. Net sales for the three months ended December 31, 2021 were $10.9 million, a 13% decrease from $12.5 million in the same period of the prior year. However, excluding the sales of FiberCel, we saw a 6% growth over the fourth quarter of 2020. In late December, as was broadly experienced across much of the healthcare sector, the Omicron variant spike had a meaningful impact on our business, which has continued into the current quarter as COVID-related hospitalizations and labor shortages in the hospital setting impacted patient's ability to move forward with procedures. And while we're starting to see improvement as patients return to hospitals for postponed procedures, we do expect it will have some impact on our sales in the first quarter. Gross margin for the fourth quarter of 2021 was 31.2% as compared to 48.3% in the corresponding prior-year period. We also look at gross margin excluding the impact of non-cash amortization of intangible assets. And on that basis, Q4 would have been 39.0% versus 55.1% in the year-ago quarter. The lower gross margin in Q4 2021 was mainly attributable to increased inventory reserves in our Human Tissue business, which in total impacted gross margin by approximately 10% points, or $1.1 million. Despite gross margins coming in below our target levels over the last two quarters, as Ronald mentioned, we have a number of efficiency initiatives that are underway and we expect them to generate meaningful results in 2022. I expect gross margin excluding intangible asset amortization to return to 50% or better in the coming quarters. Total operating expenses for the fourth quarter of 2021 were $11.2 million, a 12% increase from $10 million in fourth quarter of 2020. The increase was mainly due to development costs associated with our CanGaroo RM development program. Loss…

Thank you. And as a reminder [Operators Instruction]. One moment while we compile the Q&A roster. Question is from Matthew O'Brien with Piper Sandler Companies. Matthew O’Brien: Thanks for taking my questions. I guess Matthew, just for starters, the impact to Q1 that you're expecting in terms of Omicron softness and then how that relates to the rest of the year, getting to the midpoint of the range without RM? What are you seeing in those new accounts that give you confidence and that step-up as we get later in the year?

Sure. Thanks, Matthew for the question. We definitely did start to see some impact from Omicron as we got into December in particular last year. We have seen it, I would say so far this quarter, but it does feel like it's tapering off and things are starting to pick up again in the quarter. I guess as I think about the year, I do think about it ramping up as we go through the year kind of regardless of the benefit or the contribution that we may get from CanGaroo RM as we get into the latter part of the year. So hopefully that's helpful, I guess I would see Q1 being similar to Q4, maybe in that range. Matthew O’Brien: Got it. That's helpful. And then with RM, everybody is excited there. Can you Ronald, maybe just talk a little bit about what's you're hearing from customers as far as the anticipation of that product, the uptake. I'm sure Boston and Biotronik are excited to have it. Knowing that you're going to probably roll it out slowly and make sure that things go well. But what kind of appetite is there once you do have that, hopefully later this year? And I do have one quicker follow-up.

Sure. Thanks, Matthew. We're very excited about CanGaroo RM. And I think if we look at the product today and CanGaroo, we're actually starting to see nice momentum build on CanGaroo and is due to the remodeling benefits of having a biological product. Again, that's really resonating with customers as we speak today. And we know that when we add then antibiotics to it, we now have two benefits from a customer's perspective in terms of the patients that are able to then receive the product and have numerous benefits related to having both the biological and an antibiotic. And as I alluded to in our comments, we recently conducted some market research. Not surprisingly the physician excitement for the product was very high, with more than 80%, of the physicians indicating a desire to want to have a both a biological antibody product. So, we believe it's going to be a product that brings a lot of benefits in the marketplace. Certainly, the entire Aziyo organizations excited about that. Our partners, Boston Biotronik, are also very excited to have that as an offering as well. And again, as I mentioned earlier, we see it as a key catalysts for growth for the company going forward. Matthew O’Brien: Okay, thanks for that. Then that kind of dovetails into the last question I'll ask. But Ronald, you're talking about exciting '23, $5 million bucks is what you offer. FiberCel this year, hopefully we have a partner, for next year RM should be a contributor. Those two together seemed like they can alone be an extra $10 million bucks next year. So, you're talking about 14%, 15% midpoint growth this year excluding FiberCel. I mean, should we think of '23 as 20% plus?

I don't think we want to get into '23 guidance here from perspective of the company, but I would just want to reiterate back as what you've said. We're very excited about where we're going from a company perspective. We think there's tremendous growth opportunity with the launch of CanGaroo RM. Again, it's a $600 million marketplace. We've got really one competitor that's more than a $100 million in sales, a lot of room for market expansion. Again, the dual benefits of biologic antibodies we believe should give us tremendous opportunity to grow that brand. As you mentioned, we do have other growth catalysts. Just to mention SimpliDerm continues to perform extraordinarily well, and we continue to believe that will be a key growth component going forward. As you also mentioned, our viable bone business, we've already been able to go out and sign some additional partners already here in Q1. Again, building up our unique platform of our viable bone strategy to best preserve the cells that are inbound reducing Exostosis. We think we have the opportunity to again, bring an additional business through partnerships for them as well. I think we're excited where the company's going. We see this, as I mentioned, a breakout year for Aziyo setting up a very strong 2023. Matthew O’Brien: Thank you.

Thank you. Our next question comes from David Rescott with Truist Securities.

Hey, Ronald and Matthew. Thanks for taking the questions. Matthew, I just want to start first on the guidance from January require just some comment around the progression of procedures throughout the year and then some of the assumptions around the contribution of RM in the fourth quarter. And so just -- what level of penetration were you thinking about in the fourth quarter? And when you get to that upper end of the guidance range, should that assume that RM comes in the beginning of Q4 or maybe towards the back half of the fourth quarter?

Well, David, yeah. So, as we thought about the guidance for the year, the biggest thing that is out of our control that's difficult to predict is the timing of RM clearance and that's largely going to be in the hands of the FDA. And we feel good about the track that we're on in terms of getting the filing done and making that very high-quality filing but after that, it's a little bit harder to predict. So as we were thinking about the range, I would say the top end of the range assumes that we would have very much of a full quarter worth of contribution and we would certainly see there's also some factors in terms of ramping up production and getting on contract or getting in on the formularies within hospitals, so there are some startup effects there. But we are looking forward to that very much. And at the lower end of the range, if the clearance extends out to the very end of the year and we have minimal to no contribution for revenue for the year, that would guide us more towards the lower end of the range that we talked about.

Okay. That's helpful. And then I guess Ronald maybe more on some of the commercialization efforts or the investments you're making around that ahead of the launch, could you just discuss how you're investing in the business side of the launch? And then when you're thinking about, either in the back half of the year or into 2023, is there a lot of low-hanging fruit for RM, at least these accounts that you're currently in? And how do you think about some of this kind of increasing utilization versus going after new accounts once you have the RM formulation approved?

Yes. Sure. So, as we think about the products, I mean, clearly there's some low-hanging fruit. We have many customers that said that they would use the product if it also had antibiotics. I think there is an immediate opportunity to go there. As we think about our launch strategy here, obviously, we're in the midst of doing our launch planning. I would say that part of this is our ongoing investment on data generation as well. So, we have two studies on, running, ongoing right now, the heal study and the registry study. We hope to have this year in a readout from both studies. They'll further, I believe, better demonstrate our remodeling benefits of the product. And again, we think that's an important characteristic that further drive CanGaroo RM growth, in addition to antibiotics. So, looking forward to those readouts as well. And then again, we'll make sure that we make the right investments to be able to capitalize on this new product opportunity. And to basically look at that in totality. So, it's probably at this point, though a little premature to get into specifics as it relates to launch locked -- launch tactics. But we're going to obviously make sure we do everything we can to ensure that we have the most successful launch for this product.

That's helpful. Thanks for taking the questions.

Thank you. Our next question comes from Joshua Jennings with Cowen and Company.

Hi, this is Brian here for Joshua, thanks for taking my questions. I wanted to ask first about RM. If I look at the review times for your recent 510(k) submissions, I see that the average review time is about a month and a half. I understand wanting to keep the guidance conservative, but is there a specific reason to assume a longer review for RM? And will you be ready for an earlier launch than 4Q if you get an early clearance?

Yes. So, if you think about CanGaroo RM, it is probably a little bit more complex than your normal 510(k). Obviously, there's a device component and then there's also the drug component. So being a combination device here with the 510(k), so we anticipate probably a little bit more complex. And so, we're building a little bit more review time from that perspective. We're hopeful that maybe it goes through faster, again, we can't predict the FDA. And again, we'll do everything we can to be prepared to launch as soon as possible as it relates to the product. And certainly, having the approval sooner gives us the opportunity to go out and start promoting the benefit of CanGaroo RM from the biologic and antibiotic perspective. So, we'll be as ready as we can be for an earlier approval and hopefully the FDA, from a timing perspective, allows us to be on the early end of that approval window.

Great, thanks. And I wanted to ask one about the FiberCel recalls. So, you've commented previously that on the FDA inspection mid-last year, without any observation, is the inspection process definitively done at this point and is there now agreement that the recalls really limited to that single lot that's already been identified and acted on thanks.

Yes. The FDA inspection has been completed again, with no observations. We have moved forward as a company and we have now raised the bar above industry standards as it relates to donor screening, as well as testing of products. So, we believe we are setting a new standard as it relates to the industry. But from an FDA perspective than their inspection and the recall matter. Yes, it's contained to the single Dharwad.

Thank you. And I'm not showing any further questions in the queue. I will turn the call back to Ronald Lloyd for final remarks.

Thank you. Just to close again I think we're really proud of the progress we've made as the Aziyo team has really setting up 2022 to be our breakout year for the company. We're excited about the number of short-term catalysts that we have, which we believe put us in an excellent position for growth. And as such, we look forward to giving you updates as we go throughout the year. Thank you again for your time today. Take care.

With that, ladies and gentlemen, we conclude today's program. Thank you for your participation and you may now disconnect.