June 30, 2020 was $17.4 million, or $0.31 per share, compared to non-GAAP net income* of $23.8 million, or $0.42 per share, for the quarter ended June 30, 2019.
Merit’s revenue by category for the three and six-month periods ended June 30, 2020, compared to the corresponding periods in 2019, was as follows (unaudited, in thousands, except for percentages):
| | | | | | | | | | | | | | | | |
| | | | Three Months Ended June 30, | | | | Six Months Ended June 30, |
| | % Change | | 2020 | | 2019 | | % Change | | 2020 | | 2019 |
Cardiovascular | | | | | | | | | | | | | | | | |
Peripheral Intervention | | (18.2) | % | $ | 72,635 | | $ | 88,848 | | (7.9) | % | $ | 159,710 | | $ | 173,481 |
Cardiac Intervention | | (17.1) | % | | 66,005 | | | 79,643 | | (8.9) | % | | 138,596 | | | 152,183 |
Custom Procedural Solutions | | (4.0) | % | | 45,319 | | | 47,216 | | (0.1) | % | | 92,940 | | | 93,077 |
OEM | | (8.9) | % | | 28,218 | | | 30,959 | | (3.3) | % | | 56,475 | | | 58,405 |
Total | | (14.0) | % | | 212,177 | | | 246,666 | | (6.2) | % | | 447,721 | | | 477,146 |
| | | | | | | | | | | | | | | | |
Endoscopy | | | | | | | | | | | | | | | | |
Endoscopy devices | | (30.1) | % | | 6,194 | | | 8,866 | | (15.3) | % | | 14,175 | | | 16,735 |
| | | | | | | | | | | | | | | | |
Total | | (14.5) | % | $ | 218,371 | | $ | 255,532 | | (6.5) | % | $ | 461,896 | | $ | 493,881 |
“During the second quarter we continued to make progress on the goals we initiated in early 2019, including the movement of 14 product lines and consolidation of certain facilities,” said Fred P. Lampropoulos, Merit’s Chairman and CEO. “We are particularly pleased with the generation of free cash flow* of $32 million for the quarter and $47 million year to date.”
“We also focused on dealing with the challenges of the COVID-19 pandemic,” Lampropoulos said. “Our priority was the safety of employees. Deemed an ‘essential provider,’ we continued operation in all of our facilities worldwide by implementing CDC recommendations, including temperature testing, social distancing, mask-wearing, frequent hand-washing and installing separation barriers.”
“In order to balance the reduction of incoming sales orders due to the suspension of elective procedures by many facilities we serve, we reduced headcounts, implemented targeted furloughs, and reduced salaries for a number of groups, including all executive positions,” Lampropoulos said. “We also reduced the number of research and development projects to focus on the highest priority projects in order to reach our financial and competitive objectives.”
“During the second quarter, we received the CE mark for the Merit WRAPSODYTM Endoprosthesis Stent System, and we have initiated commercialization in the European Union,” Lampropoulos continued. “We also received approval for the WRAPSODY Arterial Venous access Efficacy (WAVE) IDE trial from the FDA. This approval will allow us to proceed on several cohorts with up to 50 institutions and more than 350 patients, in anticipation of application for the FDA’s consideration of PMA approval for commercialization in the United States. We also introduced new products that address needs in the COVID-19 environment which have had an impact in the second quarter, which we believe will offer additional opportunities.”
“We added three new directors with substantial medical device experience and have formed an Operating Committee to establish future financial and performance objectives that we plan to announce during our third quarter report in October,” Lampropoulos said.
“As recently reported, we reached an agreement with the U.S. Department of Justice to fully resolve its pending investigation,” Lampropoulos said. “Based upon that agreement, we recorded a charge of approximately $18 million during the second quarter. We intend to release additional details regarding the settlement following the finalization of the settlement documents.”
“With COVID-19 cases increasing, the pace of recovery of elective procedures is still uncertain,” Lampropoulos said. “Access to customers and opportunities to pursue clinical trials for new products are still very limited. However, we are still proceeding with new product development, clinical and regulatory activities, and marketing and training programs. Assuming eventual progress in the fight against the COVID-19 pandemic, we believe we are well positioned to provide new products and services as well as reliable supply of our existing products.”