Robert Gershon
Analyst · JMP Securities. Please go ahead
Thank you, Andrew. And thank you all for joining us this morning to review our third quarter results and discuss key developments across our organization. With me today are our CFO, Jay Ewers; and our Chief Commercialization Officer, Jack McCarthy. At the end of our prepared remarks, all three of us will be available to answer questions. This was an excellent quarter for Bovie Medical from several perspectives. We reported a double digit increase in total revenues compared to last year’s third quarter. J-Plasma sales were higher than the last two quarters combined and each of the metrics tied to future J-Plasma sales showed substantial sequential growth. Additionally, the recent progress we have made on three key initiatives has further strengthened both our core business and the potential for J-Plasma. Specifically, we reported a 15% year-on-year increase in total revenues and gross margin that was stable with the adjusted gross margin we reported in last years’ third quarter. The profitable growth of our core business has always been an important objective for us and we are continuously exploring opportunities to build our product portfolio and increase efficiencies. The big news of the third quarter, however, was J-Plasma. And as I said in the earnings release, we believe we have reached an inflection point in terms of positive sales momentum. First, our J-Plasma sales surpassed $500,000 and we have closed in on the $1 million mark for the first nine-months of this year. Of course the numbers are relatively small, but the trends are undeniable. After sales, the metric that we watch most closely is generators in use, as it has the closest co-relation to actual sales and is a good indicator of future recurring revenue from hand piece sales. In the third quarter, we had 62 generators in use at 53 hospitals in 18 states, representing an 82% sequential increase over the 34 that were in use at the end of this years’ second quarter. The install base is comprised of generators that we have sold or leased to hospitals where J-Plasma has been VAC approved, as well as generators that we have placed in hospitals where J-Plasma has been VAC approved or is still under VAC review. In the case of latter, we charge a premium for the disposable hand pieces as part of the program that allows hospitals to pay for the use of a generator without having to purchase any capital equipment. Placing the equipment on site has proven to be one-way to shorten the sales cycle and increase the number of surgeons who are exposed to J-Plasma. At the same time this has resulted in disposables representing a greater proportion of our J-Plasma sales than they generally would at this early stage of commercialization, which is fully aligned with our strategy of growing recurring revenue. 62 generators in use gives us the scale to effectively mind our installed base. Being on site, puts us in an excellent position to increase adoption amongst surgeons with access to our generators and broaden awareness within the institutions were J-Plasma is already VAC approved or in review, while continuing to expand the universe of surgeons who are using the product. At the end of the third quarter, there were 132 surgeons using J-Plasma and 74% sequential increase achieved in just a three-month time horizon. Also, we are very proud of the fact that all surgeons who have been trained by us on J-Plasma have emerged as users of the product. As we have noted previously, there is a lag time between the time, the surgeon begin using J-Plasma and when that translates into bulk purchase orders from their hospitals. This is due to the longer approval process at value analysis committees or VACs a situation that is not going to be medical specific, but rather confronting our entire industry. One mechanism we have to capture these sales is via Scrub POs, which are issued when the surgeon is using the product in the OR, while it is under VAC review. With the timing of VAC approvals increasingly unpredictable and the significant amount of paper work required following approval Scrub POs have become another accurate early indicator of future sales. In the third quarter, we received 79 Scrub POs, almost double the 42 we received in the first six months of this year, bringing the total for 9 months to a 121 compared to just 6 for all of last year. And while we are frustrated by the time it takes to complete the VAC reviews, we cannot complain with the treatment that J-Plasma is getting from them. We were approved by 17 VACs during the third quarter, bringing the total VAC approvals up to 59 year-to-date and J-Plasma was under review by an additional 64 VACs. The VACs at two large systems have deferred approval requiring that we publish ongoing clinical studies prior to their approval, but except for those two we are batting nearly a thousand. Taking all of these metrics together, it is clear that we are positioned for substantial growth in J-Plasma sales in the periods ahead, with the vast majority of demand coming from OB/GYN and plastic surgery, which has been our initial target markets. Last quarter, I discussed the formation of a medical advisory board to assist us in determining those specific procedures in other surgical specialties for which J-Plasma is well suited for broad-based adoption. Our first member, Dr. Vip Patel, a world renowned urologist and leader in robotic surgery believes that J-Plasma has the potential to significantly benefit patients undergoing surgery for prostate cancer. One of the strategic initiatives I mentioned earlier is the progress we have made in building out the Medical Advisory Board. The two new surgeon members we announced in our third quarter earnings release are at the top of their fields, Dr. Husam Balkhy, is director of robotic and minimally invasive and cardiac surgery at the University of Chicago Medicine; and Dr. Robert Cerfolio, is Professor of surgery and section chief of thoracic surgery at the University of Alabama Hospital. Doctors Balkhy and Cerfolio see multiple ways in which J-Plasma can become the standard of care for certain procedures within their respective specialties of cardiovascular and cardiothoracic surgery. In addition to expanding J-Plasma’s addressable market, we believe that expanding from OB/GYN and plastic surgery into specialties like these will accelerate the hospital VAC process. All three medical advisory board members have been working with us on J-Plasma and have collectively completed many labs and surgical cases using the products. In short order, we expect to expand the board to 6 to 9 members. Another strategic action we took since our last earnings call was to purchase Bovie, Bulgaria, our R&D and manufacturing contractor base in Sofia. This transaction gives us control over an important part of our product development activities and supply chain and we project that it will result in net cost savings of approximately $850,000 for 2016 and 2017 combined. And lastly, we continue to execute our strategy to unlock the value of the Bovie R&D pipeline. In the third quarter, we announced the receipt of FDA clearance for 6 new hand piece configurations that extend the J-Plasma pistol grip product by offering additional instrument length and adding a new needle option. The longer length allow greater surgical reach and the needle enables even more precise delivery of energy giving the surgeon added control around vital organs. Just a few days ago, we received FDA clearance for our next J-Plasma product extension, which is branded, precise, 360. This J-Plasma hand piece has a reticulating tip that will enable surgeons to navigate structures that are out of the reach using a straight laparoscopic device. And the next J-Plasma portfolio addition on the drawing board is a hand piece design specifically for use in robotic surgery, which we expect to launch in the second half of next year, and we look forward to collaborating with our Medical Advisory Board members to develop other new J-Plasma product configuration. Jay will be reviewing our third quarter financial performance in just a moment. I do want to comment however on the fact that we kept our administrative and other non-revenue generating cost in check in the third quarter and have allocated our resources to those areas where we see meaningful growth potential. We succeed in maintaining our cash position at $13.2 million just modestly below the $14.1 million in cash that we had at the end of the second quarter providing ample funds to support the commercialization of J-Plasma. At this point, I will turn over the call to Jay Ewers for a financial review of our third quarter results. Jay?