INTUITIVE SURGICAL INC quarterly report, Q2 FY2017

Business context and reporting period

Intuitive Surgical, Inc. designs, manufactures, and markets da Vinci robotic surgical systems and related instruments, accessories, and services. This unaudited Form 10-Q covers the quarter and six months ended June 30, 2017, compared with the corresponding 2016 periods. The da Vinci X launched in the U.S. in May 2017.

Key financial metrics

Amounts are in millions except per-share data, percentages, and system counts.

MetricQ2 2017Q2 2016Six months 2017Six months 2016
Total revenue$756.2$670.1$1,430.4$1,264.6
Gross profit$527.9$470.9$994.0$875.9
Gross margin69.8%70.3%69.5%69.3%
Operating income$257.5$245.4$449.0$424.4
Net income$221.5$184.5$401.3$320.9
Diluted EPS$5.77$4.71$10.42$8.25
Operating cash flowNot reported quarterlyNot reported quarterly$458.0$488.5
  • Q2 revenue increased 13%; net income increased about 20%. First-half revenue increased 13%; net income increased about 25%.
  • Q2 product revenue was $614.2 million and service revenue $142.0 million. Recurring revenue was $539.8 million, or 71% of total revenue, up 15% year over year.
  • Q2 instrument and accessory revenue grew 17% to $397.8 million; systems revenue grew 7% to $216.4 million. The company shipped 166 systems versus 130 a year earlier; installed base reached approximately 4,149.
  • Q2 operating expenses rose to $270.4 million from $225.5 million, including R&D expense of $84.6 million versus $54.7 million. Service gross margin declined to 69.0% from 73.9%; product gross margin improved to 70.0% from 69.4%.
  • At June 30, cash and cash equivalents were $696.5 million; short- and long-term investments totaled $2.727 billion. Combined cash and investments were approximately $3.4 billion, down from $4.8 billion at year-end 2016. Total liabilities were $728.5 million; the balance sheet shows no debt line item.
  • First-half investing cash flow was positive $954.5 million, mainly reflecting net investment sales and maturities. Financing cash flow was negative $1.754 billion, primarily from a $2.0 billion accelerated share repurchase. Operating cash flow was $458.0 million.

Material changes versus the prior comparable period

  • Global procedure volume grew approximately 16% in Q2 and 17% in the first half. First-half U.S. procedure growth was about 14%; outside the U.S. it was about 25%.
  • Revenue growth was led by recurring instruments, accessories, and services, supported by higher procedure volume and a larger installed base. System shipments also increased, though system average selling prices fell: approximately $1.46 million in Q2 versus $1.56 million a year earlier, excluding operating leases.
  • R&D spending increased substantially to support a broader development pipeline. Management expects R&D expense to continue increasing.
  • First-half operating cash flow declined from $488.5 million to $458.0 million, with working-capital uses including higher receivables, inventory, and prepaid expenses.
  • Reported tax rates fell to 17.2% in Q2 and 14.2% for the first half, largely due to the new accounting treatment for employee share-based tax benefits. Those benefits reduced the effective tax rates by 11.4 and 13.5 percentage points, respectively.

Outlook, management commentary, risks, and unusual items

  • The filing provides no specific revenue, earnings, or procedure-volume guidance. Management says available cash, investments, and expected operating cash generation should meet liquidity needs for the foreseeable future.
  • Management identifies procedure adoption, hospital capital spending, reimbursement, regulatory clearances, competition, and product acceptance as drivers of future demand. China system placements depend on new import authorizations or public-hospital quotas and tender processes; timing is uncertain. Further Japanese procedure reimbursements are also uncertain.
  • A first-quarter customer trade-out offer for the da Vinci X resulted in $23.4 million of revenue remaining deferred at June 30. The company anticipated the rights would be substantially resolved before year-end 2017.
  • The $2.0 billion accelerated share repurchase materially reduced cash and investments; $991.6 million remained authorized for repurchases at June 30. Final ASR settlement was scheduled by Q4 2017.
  • Product-liability settlement charges were $16.0 million for the first half, and accrued liabilities for tolled claims were $32.9 million at June 30. The company says additional losses are reasonably possible but cannot estimate an excess range. A shareholder securities class action and derivative suits remained pending or subject to settlement approval; the company did not expect material adverse effects from these matters.
  • The company received $10.0 million from an insurer settlement in June 2017. Separately, Ethicon filed a patent-infringement complaint concerning EndoWrist Stapler instruments on June 30, served July 12; the company could not estimate a loss or range.
  • A 2017 accounting change caused excess share-based compensation tax benefits to be recognized in earnings and is expected to increase tax-rate volatility. Adoption of the new revenue standard was planned for Q1 2018, with full retrospective application anticipated; the company expected no material impact but had not completed its assessment.
  • The 60%-owned Fosun joint venture was legally formed in Q2 to develop and commercialize catheter-based robotic medical devices. The company expects startup losses and no joint-venture revenue in 2018; successful development, commercialization, and funding are uncertain.

Important facts for investors to verify

  1. Whether procedure growth, particularly in general surgery and international markets, continues to support recurring revenue and system demand.
  2. Whether the da Vinci X launch affects system placements, average selling prices, and recognition of the $23.4 million deferred trade-out revenue.
  3. Whether higher R&D and service repair costs, litigation charges, and tax-benefit volatility change operating margins or reported earnings.
  4. Whether the accelerated repurchase’s final share settlement and any further buybacks materially affect liquidity and share count.
  5. Developments in product-liability claims, the Ethicon patent case, shareholder litigation, China authorizations, and the Fosun joint venture.