Good day, and thank you for standing by. Welcome to the Nano-X Imaging Second Quarter 2022 Earnings Call. At this time, all participants are in a listen-only mode. After the speakers’ presentation, there will be a question-and-answer session. [Operator Instructions] Please be advised that today's conference is being recorded. I would now like to hand the conference over to your speaker today, Mike Cavanaugh, Managing Director of Investor Relations. Please go ahead.

Good morning, and thank you for joining us today. Earlier today, Nano-X Imaging Limited released its financial results for the quarter ended June 30, 2022. The release is currently available on the Investors section of the company's website. Erez Meltzer, Chief Executive Officer; and Ran Daniel, Chief Financial Officer, will host this morning's call. Before we get started, I would like to remind everyone that management will be making statements during this call that include forward-looking statements regarding the company's financial results, research and development, manufacturing and commercialization activities regulatory process operations and other matters. These statements are subject to risks, uncertainties and assumptions that are based on management's current expectations as of today and may not be updated in the future. Therefore, these statements should not be relied upon as representing the company's views as of any subsequent date. Factors that may cause such a difference include, but are not limited to, those described in the company's filings with the Securities and Exchange Commission. We will also refer to certain non-GAAP financial measures to provide additional information to investors. A reconciliation of the non-GAAP to GAAP measures is provided with our press release, with the primary differences being goodwill impairment, change in obligation in connection of the merger and acquisitions, stock-based compensation, amortization of intangible assets and class action litigation and SEC and COVID-related expenses. I'd now like to turn the call over to Erez Meltzer.

Thank you, Mike, and thank you all for joining us the call today. As always, we appreciate your continued support of Nano-X. As in our last call, I will give an overview of our recent achievements and share our outlook on the coming months before turning the call over to Ran Daniel, our Chief Financial Officer to review our financial results. We will then open the call up to questions. We've continued to make progress during the past quarter to advance the Nano-X ARC system towards commercialization and we continue to proceed full force ahead to make headway in the FDA clearance process. On the call today, I will discuss the advances we have made since our last earnings call by breaking my comments into three distinct segments: regulatory, commercialization and finally AI and teleradiology. I will discuss what we have done in each of these segments and how we have moved closer to our goal of system deployment at scale. Before I do that, I'll touch on our financial results at a high level, but we'll leave most of the details to Ran’s commentary later in the call. Nano-X generated top line revenue of $2.2 million in the second quarter of 2022, compared to $1.8 million in Q1 2022. As in the previous quarter, all revenue was generated by Nano-X teleradiology services business unit and by Nano-X AI, our deep learning machine analytics company. As most of you know, these business units began generating revenue since their acquisitions in November 2021, and it's gratifying to see our teleradiology services growing quarter-over-quarter. These revenues were relatively small at this time are important for two reasons: First, they help us to improve our cash flow and its management. And second, we believe they demonstrate that customers and other stakeholders such as…

Thank you, Eric. First, I'm delighted to announce that we were added to the Russell 2000 and Russell 3000 Indexes, effective after the U.S. market opened on June 27th as part of the 2022 Russell indexes annual reconstitution. This is a great development for our company. As for our financial results, we reported a GAAP net loss for the second quarter of 2022 of $19.6 million, compared to a net loss of $13.6 million in the second quarter of 2021, largely due to expenses related to the acquisition of the Nano-X market platform in November 2021. The consolidation of Nano-X AI and USARAD with the company since the fourth quarter of 2021 and increasing our research and development expenses, goodwill impairment and increase in our general and administrative expenses, which was mitigated by decrease in our sales and marketing expenses and a decrease in our obligation in connection of merger and acquisitions. Our revenues for the second quarter of 2022 were $2.2 million and gross loss was $1.8 million, revenue from teleradiology services for the period was $2.1 million with a gross profit of $0.0 million. On a GAAP basis and a gross profit of $0.9 million, on a non-GAAP basis, which represents gross profit margins of approximately 43% on a non-GAAP basis. Revenue from licensings of AI solutions for the period was $0.1 million with a gross loss of $2.1 million on a GAAP basis and $0.1 million on a non-GAAP basis. Research and development expenses for the second quarter of 2022 were $6.5 million, compared to $4.3 million for the comparable period in 2021. The increase in our research and development expenses was mainly due to consolidation of Nano-X AI with the company since November 2021, increasing our share-based compensation and the balance due to the development of…

Thank you, Ran for the financial update. And once again, thank you all for joining us today. I feel very good about Nano-X results in the second quarter as CEO. But all of us recognize there is more to do. We hope to provide additional updates in the coming weeks and months. I would also like to share with you all that the Nano-X management team will have a non-deal roadshow with investors in late September, if you would like to schedule a meeting, please contact our Investor Relations partners at ICR. With that, I'd like now to open the call for questions. Operator, please begin the Q&A session.

Thank you. [Operator Instructions] Our first question comes from Jeff Cohen with Ladenburg. Your line is now open.

Hi, Erez and Ran. How are you?

Great and yourself?

Just fine. Couple of questions from our end. So could you talk about the technology center you're planning on opening at Israel and the capabilities that you anticipate there versus the current and anticipated capabilities in the facilities in Korea and Japan?

First of all the -- it's going to be very similar, but we're going to strengthen the fact that we are willing to base our future on further advanced technologies. Right now, we have both centers in Japan and in Korea for the chips and the tubes. We thought that it would be appropriate that the core technology and knowledge will be developed very close to where we do the R&D, the product design, the roadmaps, our future products, et cetera. And that Korea will be a kind of more of manufacturing and supply for the chips and further development that will be on the engineering side.

Okay, got it. Could you talk about ARC manufacturing and number of ARCs, which have been manufactured and maybe anticipated number of ARCs manufactured by the end of the year? And then tie that into your anticipated timeline at the FDA as far as your product today?

Okay. So first of all, we are accelerating the production as mentioned. Obviously, we're not disconnected from the reality of the -- what's going on in the market in terms of the supply chain, in terms of the various components, which are part of this assembly. So we have actually part of the systems will be pushed to 2023 to hopefully for the beginning. And this is with respect to the production we are -- even before the end of the year, we are going to go even to the next step to further explore the discussion with the mass production, and I mean beyond the 1,000 units in one or two locations, which are not in Israel. We mentioned that the first 1,000 units will be assembled in Israel and we hope that either Q4 or Q1 next year, we will have the arrangement for the assembly of all the systems falling after the first 1,000 units. With respect to the question that you asked about the FDA. First of all, I was very happy with the meeting that was held last week, which was actually the last -- not the last, but the last meeting before the final preparation for this submission. I would say that the feedback that we received from the FDA was very helpful and meaningful for us. So as we say we are in the final preparation for the formal submission and it's going to be aligned with our path moving forward. Right now, I would say that the idea to go to the pre-sub into the Q submission and to take the advantage for -- I would say, about eight almost eight months dialogue, continuous dialogue with the FDA and proven itself to be the right decision. And I think that all the feedback that we got and the cooperation that we are -- that we had with FDA and we continue to have with the FDA will make it much easier for us to do it, so --

Got it. And then finally, talk about Ghana as far as manufacturing and delivering ARC units. How many would you expect to be delivered there in the coming quarter or two?

Right now, I would say that the -- we explained in the past that basically not all the countries that we're working in require the FDA regulation, like we mentioned, Nigeria, one of them and Ghana will be another one. We have another two that are not really related to the submission of the -- to the formal approval of the FDA. Ghana has a special process that we are going through, they gave us indications, but I wouldn't actually -- until I see it in my eyes, I wouldn't actually commit to -- we hope to have the approval to send the systems during the fourth quarter. And I would say the starting gun next year, it will be probably more system that will be sent. Overall, the agreement is for 350 units.

Got it. And then one quick question for Ran. Would you expect any goodwill impairment on the back half of the year for Q3 or Q4?

But as we say in the PR, it really depends on the market parameters, but the interest rate, yes there will be an increase or there will be any change in other capital market formats. So we may have to do an impairment again, we have to test it at least. And it also depends on our internal management estimate.

Okay, perfect. That does it for us. Thanks for taking the questions.

Thank you, Jeff.

Thank you, Jeff.

Thank you. Our next question comes from the line of Suraj Kalia with Oppenheimer. Your line is now open.

Good morning, Erez, Ran. Can you hear me alright?

Loud and clear.

Perfect.

Perfect. Hope everyone is safe and healthy. Hey, so, Erez, just following up on Nanox.ARC the multisource submission. Was a full power level ever in doubt, maybe I'm misreading from your comments on the feedback from the FDA. If I remember correctly, last quarter, I think so you all had mentioned that from 40 to 120 KvP, it would cover the entire gamut. So maybe if you could kindly shed some additional light on your specific comments at the full power level feedback?

First of all, I hope that I understand the question, but it has never been a doubt.

Okay, fair enough. So, Ran, when -- are you at -- or can you give us a timeframe as to when the multisource 510(k) will actually be filed? And when you're expecting clearance?

As you already know, I'm actually -- I can say or indicate or willing to commit only things which are 100% sure that there will be on the time that I'm actually committing. So right now, I think that I gave enough background and information about the timeline. We are in the final preparation to the submission and it will be done shortly. And I think that the -- this is -- I would say, positively think the feedback that we got from the FDA gave us the advantage to add a few things in the submission that will be done in the next few weeks that will be added to the system. So I hope that this submission will be -- will then shortly. And once it's submitted, I'm sure that you'll know about it.

So you will file more than likely in Q4?

You said so? Basically, I'm always trying to do things earlier on all level and all fronts.

Erez, the CE Mark, generally speaking, companies have voiced a lot of concern, just the MDR process has become very cumbersome. CE process has overall become very cumbersome and maybe I missed it in your prepared remarks on the updated timelines for CE Mark for Nanox.ARC multisource?

First of all, we have already submitted all the necessary documentation for the registration with the notified body. We have selected the notified body, we gave them all the information. You know the -- when I was a young guy, I learned that, that you have to do, whatever you can, when you can control things. You have to be patient when you cannot, but you hope that you will have the wisdom to differentiate between them. This is basically right for the CE and for the FDA. We can't control what we are doing, okay? We cannot control -- we are not managing the CE or the FDA. And we hope that the fact that they have a lot of overload in their systems and processes will not hurt us and will give us the privilege that the preparations that we have done during the last few months, we'll give the results sooner rather than later.

Got it. Erez two final question, I'll hop back in queue. So in terms of Ghana, what do our validation testing has been done before you'll start shipping these units? And the second -- the last question from my side Erez is, the 6,850 units that you referenced in terms of contractual amounts. If memory serves me right, a substantial portion of these or more than three year old contracts, I remember seeing these in 2019. Maybe if you could just talk to us about whether they are still valid or have there been any amendments? Any additional color there would be greatly appreciated? Gentlemen, thank you for taking my questions.

Okay. So first of all, I'm not sure about the first question about the validation. What exactly are you referring to with respect to the systems that we check the answer is yes. So I would say positive to the second question. With respect to the clearance in the region, are you referring to what kind of validation in terms of technology or in terms of regulation in Ghana?

No, Erez what I meant was before you launch any product commercially, you have to go through a slew of testing, performance testing [Multiple Speakers]

Yes, yes, of course. Yes, yes. The answer is basically yes. Not basically the answer is yes.

Okay. Thank you.

Thank you. Our next question comes from the line of Rahul Rakhit with LifeSci Capital. Your line is now open.

Hey, guys. Thanks for taking the question. So you mentioned that there are two other countries that don't necessarily require FDA clearance for deployment. Maybe if you could talk about where you are in conversations in those geographies and provide any indication on timing there?

The answer is no, because since we have not announced it to the public, as soon as we are going to announce that the public will actually share. My preference would be that only when we signed agreements we let the market know that they were signed. In the past, you know that in the 20-F there are a few countries which are -- do not necessarily need the FDA.

Right, right. Okay, that makes sense. And then really excited to hear about some of these AI agreements that you guys announced. Maybe could you help us think about the broader revenue potential there. I mean, it's obviously big health systems, what is the integration like -- what does integration look like there? And ultimately what is the broader revenue opportunity?

So first of all, with respect to the integration, I think we mentioned this in the script in the 6-K that these are -- we have already implemented in a few and installed the system over there. And we are -- and there is a timeline right now in the next few months. I think the last one is going to be October and November I think, November. November will be the last one that we're going to install the system in all the hospitals that, that this specifically in Northwell gave us to as part of the plan. In terms of IBM in general, our business model is basically that it can go. And this is by the way unlike what used to be in the past and in the old, what used to be Zebra Medical. Right now, it's everywhere between a few $100,000 to a few million dollars in scale.

Got it. Okay. I appreciate that. And then just based on a lot of the Q&A so far, it sounds like the conversations with the FDA been very fruitful. I know you don't want to lock in on a specific timing for the submission. But maybe can you help us understand what the impact of these conversations in the Q submission has had on the actual timing of the decision. So once you do submit the 5-K filing, how long do you expect it to take to actually obtain FDA clearance from there?

So basically, the one thing I would say, ideally in a reasonable logical market and timeline, I would say, the Q submission would be probably unworth for us, because it's very helpful in the process to accelerate the process. But right now, we know that the FDA based on the dialogue, we know that since we are working with them and cooperate with them, we know the overload that they have and I hope that it will not -- that it will give us the -- I would say, the benefit or the -- I wouldn't say the privilege, but I would say the benefit of the process that we have done to make it sooner rather than later, and that's what I was mentioned. Overall, I think the process would have had a positive impact on the process that I hope it will be the same on the clearance process.

Got it. Makes sense. Appreciate it.

Thank you. That's all the time we have for questions today. I'd now like to turn the call back over Erez Meltzer for closing remarks.

So sorry. So once again, I'd like to thank you all for being part of this call today. We'll see you shortly for those of you who are in the U.S. sometimes in September, at the end of September. And we're always at -- with ICR are willing to address any question that will -- may come from investors or from any audience that question that are related to what we're doing and what we were doing so far. Thank you so much and for the day.

This concludes today's conference call. Thank you for participating. You may now disconnect.