MILESTONE SCIENTIFIC INC. quarterly report, Q3 FY2015

Milestone Scientific Inc. — Q3 2015 Form 10-Q

Reporting period: Three and nine months ended September 30, 2015; comparisons are to the same periods in 2014. The company sells computerized local-anesthesia delivery products and is pursuing medical applications of its CompuFlo technology. It uplisted to NYSE MKT in June 2015.

Financial results

MetricQ3 2015Q3 2014Nine months 2015Nine months 2014
Revenue$2.46 million$2.54 million$7.00 million$7.66 million
Gross profit / margin$1.67 million / 67.7%$1.71 million / 67.3%$4.70 million / 67.1%$5.04 million / 65.7%
Operating income (loss)$(0.84) million$(0.16) million$(2.32) million$0.21 million
Net loss attributable to Milestone$(1.57) million$(0.36) million$(4.06) million$(0.33) million
Operating cash flow—$(3.76) million$(0.003) million

Q3 basic and diluted loss per share was $0.07, versus $0.02; nine-month loss per share was $0.19, versus a reported $0.00. Nine-month SG&A rose to $6.97 million from $4.75 million, exceeding revenue for the period. The company attributed increased costs mainly to compensation and travel, legal expenses, a consultant commission connected with a Polish grant, and expanded sales and marketing activity. Equity-method losses from Milestone Medical were $1.57 million for the nine months, versus $0.57 million; Milestone China also recorded a loss.

Liquidity and financial position

At September 30, cash and equivalents were $4.39 million, working capital was $11.14 million, total assets were $14.06 million, and current liabilities were $2.13 million. Cash declined $5.98 million from year-end 2014. The filing reports no conventional debt balance; it does report a $2.0 million note receivable from Milestone Medical. The related-party credit line was increased to $2.5 million in September 2015, and the note bears 3.25% interest. The company received a $0.5 million capital contribution from a noncontrolling interest during the period.

Changes, outlook, and risks

  • Nine-month revenue fell 9%, mainly due to lower domestic handpiece sales following price increases and distributor inventory sell-through. International revenue increased, including instrument shipments, but foreign-exchange effects and handpiece declines weighed on sales.
  • Management said cash reserves, receivable collections, and expected repayment of the Medical note should cover anticipated obligations for the next 12 months. It expected the $2.0 million note to be repaid in Q4 2015 or Q1 2016 through a planned Polish capital raise; repayment is not assured by the filing.
  • A consortium led by the company’s Polish subsidiary was awarded a $4.2 million Polish government grant, of which the subsidiary is expected to receive approximately $1.5 million. The filing describes a commission expense related to obtaining the grant.
  • The U.S. healthcare distribution partnership for CompuFlo epidural applications ended in June 2015 after delays in FDA clearance. Medical instrument development continued; the filing reports CE certification and new Polish and Italian distribution agreements, with shipments beginning in September.
  • Key risks include recurring operating losses and cash use, reliance on a small number of distributors and customers, related-party transactions and receivables, and dependence on contract manufacturers. The filing cautions that replacing a manufacturer could cause expense and delay. Two customers represented 40% of nine-month sales; three customers represented 69% of period-end receivables.
  • The company reported effective disclosure controls and no material change in internal control over financial reporting. It reported no legal proceedings at quarter-end, although MD&A discusses distributor litigation settled during 2015.

Important facts for investors to verify

  • Whether Milestone Medical repaid the $2.0 million note and whether the anticipated Polish financing and grant proceeds were received.
  • Subsequent revenue, handpiece demand, pricing effects, foreign-exchange exposure, and customer/distributor concentration.
  • Progress on FDA clearance, medical product commercialization, and the economics and timing of the new distribution agreements.
  • Cash burn and expense trends, including the sustainability of SG&A and grant-related costs; the cash flow statement reports operating cash use of $3.76 million, while a note contains an inconsistent, unclear figure.
  • Terms and potential dilution from the 7,000 outstanding Series A preferred shares, convertible at stated prices and subject to a 2019 conversion provision.