INTEGRA LIFESCIENCES HOLDINGS CORP quarterly report, Q1 FY2015

Integra LifeSciences Holdings Corporation — Q1 2015 Form 10-Q

Business context and reporting period

Unaudited results cover the three months ended March 31, 2015, compared with the same period in 2014. Integra is a medical technology company serving orthopedic extremity, neurosurgery, spine, reconstructive and general surgery markets. Beginning in 2015, the Company reported three global segments: Specialty Surgical Solutions, Orthopedics and Tissue Technologies, and Spine.

Key financial metrics

MetricQ1 2015Q1 2014Change
Revenue$233.7 million$215.1 millionUp 8.7%
Gross profit$146.9 million$132.7 millionUp 10.8%
Gross margin62.9%61.7%Up 120 bps
Operating income$16.8 million$8.7 millionUp 92.1%
Net income$8.4 million$2.2 millionUp $6.2 million
Diluted EPS$0.25$0.07Up $0.18
Operating cash flow$31.6 million$11.3 millionUp $20.4 million

Operating margin was approximately 7.2%, compared with 4.1% in the prior-year quarter. Net margin was approximately 3.6%, compared with 1.0%. The effective tax rate declined to 33.5% from 44.5%, primarily because Q1 2014 included $0.8 million of foreign and state tax audit settlement expense.

At March 31, 2015, cash and equivalents were $79.9 million, compared with $72.0 million at December 31, 2014. Working capital was $395.1 million. Carrying debt consisted of $401.9 million under the Senior Credit Facility and $215.2 million of convertible securities. Approximately $498.1 million remained available under the credit facility, and the Company was in compliance with its covenants.

Segment and operating developments

  • Specialty Surgical Solutions revenue was $140.1 million, up 10%, supported by MicroFrance, dural repair, neuro critical care and instruments; tissue ablation declined.
  • Orthopedics and Tissue Technologies revenue was $61.4 million, up 12%, supported by Metasurg, regenerative technologies and upper-extremity products.
  • Spine revenue was $32.2 million, down 3%, reflecting pricing pressure, delayed product launches and slower distributor additions.
  • U.S. revenue was $181.0 million, or 77% of total revenue. Foreign exchange reduced sales by approximately $5.8 million year over year.

Material changes versus the prior comparable period

  • Q1 2015 included revenue of approximately $5.8 million from MicroFrance and $1.6 million from Metasurg. Q1 2014 included a full quarter of Confluent Surgical revenue of approximately $14.1 million; Q1 2015 included approximately $17.7 million.
  • Operating performance benefited from increased sales of higher-margin products and improved regenerative-product manufacturing utilization.
  • Operating expenses increased 5% to $130.2 million, while operating expenses as a percentage of revenue declined to 55.7% from 57.6%.
  • The Company incurred $4.8 million of Spine separation costs in Q1 2015 and expects additional separation costs during 2015.
  • Goodwill was reallocated following the segment realignment. The Spine reporting unit recorded a $0.4 million goodwill impairment charge.
  • Comprehensive loss was $15.7 million versus comprehensive income of $3.2 million, primarily due to a $24.4 million foreign-currency translation loss.
  • Net cash used in financing was $13.8 million, including a $15.0 million repayment of revolving debt. Q1 2014 included $235.0 million of acquisition-related borrowings.

Guidance, outlook, risks and unusual items

  • Management expects 2015 gross margin of 62.0% to 62.5%, research and development expense of 5.5% to 6.0% of revenue, selling, general and administrative expense of 47.5% to 48.0% of revenue, and an effective tax rate of approximately 29% to 30%.
  • Planned 2015 capital expenditures are $40 million to $45 million. Management also expects to provide $40 million to $50 million of cash to the Spine business and spend approximately $20 million on separation-related professional fees and infrastructure.
  • The planned tax-free Spine spin-off was expected in the second half of 2015, subject to regulatory approvals, tax assurances, an effective Form 10 registration statement and Board approval. Completion and timing were not assured.
  • The Company filed an FDA Premarket Approval Supplement for its diabetic foot ulcer product and anticipated potential commercialization in mid-2016, assuming FDA approval and timely publication of clinical data.
  • Special charges totaled $16.8 million, including ERP implementation, structural optimization, severance, acquisition-related charges, impairment, convertible-debt non-cash interest and Spine separation costs.
  • Risks include foreign-currency volatility, dependence on regulatory approvals and reimbursement, product liability and litigation, acquisition integration, goodwill and intangible-asset impairment, debt refinancing, and execution of the Spine separation. The Company also has contingent consideration with a fair value of $22.1 million and uncertain tax benefits of $1.1 million, excluded from the contractual-obligations table.
  • The FDA warning letter relating to the Añasco facility was closed effective January 14, 2015. The Andover, UK facility was closed and removed from the FDA-registered facility list on December 31, 2014.

Important facts for investors to verify

  • Progress, final costs, financing and tax treatment of the planned Spine spin-off.
  • Whether reported revenue growth persists after accounting for MicroFrance, Metasurg and Confluent Surgical acquisition contributions.
  • Foreign-exchange effects, particularly the euro, and their impact on revenue and margins.
  • Availability and refinancing plans for the $230.0 million convertible notes due in 2016 and the Company’s other borrowings.
  • FDA approval and reimbursement prospects for the diabetic foot ulcer indication.
  • Future goodwill or intangible-asset impairment risk, especially for the Spine business.