Synovis Life Technologies, Inc. (ticker: SYNO, exchange: NASDAQ Global Market (.O))
News Release -
25-Feb-2009
Synovis Life Technologies Reports 19 Percent Revenue Growth for Fiscal 2009 First Quarter; Diluted EPS Increases 55 Percent to $0.14 from $0.09Veritas(R) and Peri-Strips(R) Product Lines Generate Robust Growth; Gross Margins Rise
ST. PAUL, Minn.--(BUSINESS WIRE)--Feb. 25, 2009--
Synovis Life Technologies, Inc. (Nasdaq: SYNO), today reported record
revenue and strong net income performance for the first fiscal quarter
ended January 31, 2009.
For the 2009 first quarter, net revenue rose to $13.4 million, a 19
percent increase over $11.3 million in the year-ago period. The company
reported first-quarter net income of $1.7 million, or $0.14 per
diluted share, up from net income from continuing operations of $1.2
million, or $0.09 per diluted share, in the year-earlier period.
Richard W. Kramp, Synovis Life Technologies’ president and chief
executive officer, commented on the quarter: “We are pleased to post
very strong revenue overall, most notably in our Peri-Strips®
and Veritas® product lines, which rose 25 percent and 86
percent, respectively, over the same quarter a year ago. We remain
enthusiastic about the rapid market adoption of the Veritas product
line. We believe expanding clinical experience with Veritas, combined
with strong sales focus, are responsible for the year-over-year growth.
To position Synovis for sustained growth going forward, we are committed
to investing in both R&D studies that compare competitive product
performance versus Veritas, as well as clinical studies to build the
product’s published record of clinical performance. Also important is
that we have a strong balance sheet with $65.1 million of cash and
investments and no debt, giving us the resources to prudently pursue
strategic acquisitions to leverage the growing strength of our sales
force and augment organic growth.”
Gross margin rose to 70 percent in the first quarter, a three-percentage
point gain over the first quarter of fiscal 2008. Factors driving the
improvement include: increased sales of higher-margin Veritas and
Peri-Strips products; improved labor and material utilization; and
higher average net sales prices. SG&A expenses increased 12 percent due
to higher clinical, new business development and legal costs, as well as
greater sales and marketing costs associated with the expansion of
Synovis’ sales force. The company added six new sales representatives in
the first quarter as planned: four sales people were added to the
surgical sales force and two sales people joined the microsurgical sales
team. Further, Synovis plans to hire eight more sales professionals by
the fiscal year-end. Research and development expenses rose 25 percent
over the year-ago period, primarily due to project activities supporting
the development of the Flow Coupler, in addition to current and future
indications for Veritas. Operating income for the first quarter totaled
$2.2 million, up 75 percent from operating income of $1.3 million a year
earlier.
As previously announced, the company completed the sale of substantially
all of the assets of its interventional business on January 31, 2008.
Operating results for the interventional business are reflected as
discontinued operations for all periods presented. The company recorded
a net gain of $5.3 million on the transaction in the first quarter of
fiscal 2008.
High-Potential Products Spearhead Growth
Synovis offers a full product portfolio which includes tissue-based
products, devices for microsurgery, and surgical tools and instruments
with applications in several surgical specialties, including bariatric,
general, vascular, neuro, micro and reconstructive surgery.
Product-related highlights follow.
Peri-Strips Dry, or PSD, product sales reached $4.9 million
in the first quarter, a 25 percent increase over the year-ago period due
to strength both domestically and in Europe. PSD is a bovine
pericardium-based staple-line buttress used primarily to control
bleeding and leakage of gastric fluids in bariatric procedures to treat
obesity. Peri-Strips products have an exceptionally low adverse event
rate.
Kramp said, “A record number of Peri-Strips units were sold in the
just-completed quarter. The growth in Peri-Strips sales for gastric
bypass surgery is exceeding the rate of procedural growth – a strong
indication that we are taking competitive share as well as converting
surgeons who have historically not used a buttress to using Peri-Strips
during their procedures. Interest in bariatric surgery is growing as
physicians and patients see the significant benefits of the surgery,
including substantial and sustained weight loss, a high rate of diabetes
remission, and reduction in breast and colon cancers. Gastric bypass, or
Roux-en-Y, surgery remains the most-often performed bariatric procedure
in the United States and is growing in Europe due to disappointing
long-term results with gastric banding. In obesity surgery, Peri-Strips
are particularly valued for preventing blood and gastric fluid leaks,
thus avoiding extremely costly complications.”
Revenue from patch products based on Synovis’ unique Veritas remodelable
biomaterial rose to $1.5 million in the first quarter, an 86-percent
increase over the comparable period last year. Veritas, which is
extremely strong and supple, acts as a “scaffold” to facilitate tissue
regeneration. Synovis launched Veritas into the complex ventral hernia
repair market in early fiscal 2007.
Regarding the hernia market, Kramp added, “Veritas is an extraordinary
biomaterial and with it, we are capturing market share in this intensely
competitive market. Our annualized sales rate of $6.0 million is up 28
percent from our fiscal 2008 fourth quarter rate. In support of our
future Veritas sales, we are investing as planned in additional in vivo
and clinical studies to document the comparative strengths of Veritas
versus its biological competitors, and to more fully assess factors that
could affect patient outcomes. These studies will run from one to three
years with interim data expected to be available. They are a critical
and needed investment to establish Veritas as a major ‘best-in-class’
player in the complex ventral hernia market.”
Sales of the established Tissue-Guard line of products for the vascular,
thoracic and neuro applications increased by 9 percent to $3.7 million
in the first quarter, with solid growth in both U.S. and international
markets. Approximately three-quarters of the growth was due to higher
unit sales with the remainder due to higher selling prices.
First-quarter revenue from the company’s microsurgical product line was
$1.8 million, a 2 percent increase over the same period last year. Sales
of the Coupler, the primary microsurgery product, showed a 14 percent
revenue gain over the year-ago quarter. The Coupler facilitates
connecting extremely small blood vessels in about one-fourth of the time
required by hand suturing. The connection is performed in such a way
that no foreign material is placed in the blood flow path, thus
resulting in short- and long-term patency rates which compare favorably
to hand suturing. The Coupler is most often used in perforator flap
surgery – a breast reconstruction procedure performed after cancer
surgery. This procedure is reimbursed and increasing in frequency.
Kramp noted, “After many quarters of exceptional revenue growth,
microsurgical revenue was essentially flat quarter over quarter. We are
assessing likely causes and believe several factors detracted from this
quarter’s performance. There appears to have been some customer
inventory build-up in the last half of fiscal 2008 as we worked through
some back order issues for our Coupler products. Reduced capital
equipment purchases by hospitals slowed sales of the premium S&T
instruments Synovis distributes, and we are also aware of several
hospital delays in launching new microsurgical programs due to the
current economic environment. From an organizational standpoint, we had
turnover in two of our microsurgical sales territories which diverted
sales management’s time as we focused on recruiting qualified
replacements. We currently have seven sales professionals focused on
microsurgical sales and plan to increase that number to nine by the end
of our second fiscal quarter. Our micro products require a highly
technical sales approach, and it takes time to recruit and train new
sales representatives and for them to build rapport with the
micro-surgeons in their respective territories.”
Balance Sheet and Cash Flow
Synovis had $29.0 million in cash and cash equivalents, as well as $3.0
million in restricted cash and $33.1 million in short- and long-term
investments (inclusive of $5.3 million of auction rate securities), for
a total of $65.1 million as of January 31, 2009, down from $74.8 million
at the fiscal 2008 year-end. During the first quarter, the company used
cash of $8.1 million to repurchase 496,000 shares of its stock at an
average price per share of $16.39. The company has now completed the
repurchase of all 1 million shares that its board authorized in May 2008
at a total cost of $16.7 million. Operating activities used cash of
approximately $200,000 in the first quarter of fiscal 2009, consistent
with prior years, as year-end accruals for stock repurchases, sales
commissions and incentive compensation were paid in the first quarter.
The estimated fair value of the company’s $9.0 million investment in
auction rate securities was $5.3 million as of the end of the first
quarter, compared to $6.6 million as of the end of fiscal 2008. Based on
the facts and circumstances as of January 31, 2009, the company believes
fair value adjustment to be temporary and has recorded the loss as
“accumulated other comprehensive loss” in the equity section of the
balance sheet. As such, the fair value adjustment had no impact on net
income or earnings per share in the quarter.
Conference Call and Webcast
Synovis Life Technologies will host a live webcast of its fiscal
first-quarter conference call today, February 25, at 10 a.m. CT to
discuss the company’s results. To access the live webcast, go to the
investor information section of the company’s Web site, www.synovislife.com,
and click on the webcast icon. A webcast replay will be available
beginning at noon CT, Wednesday, February 25.
If you prefer to listen to an audio replay of the conference call, dial
(888) 286-8010 and enter access number 65120186. The audio replay will
be available beginning at 1 p.m. CT on Wednesday, February 25, through 6
p.m. CT on Friday, February 27.
About Synovis Life Technologies
Synovis Life Technologies, Inc., based in St. Paul, Minn., is a
diversified medical device company that develops, manufactures and
markets medical devices for the surgical treatment of disease. The
company’s products include implantable biomaterials for soft tissue
repair, devices for microsurgery and surgical tools – all designed to
reduce risks and/or facilitate critical surgeries, improve patient
outcomes and reduce healthcare costs. For additional information on
Synovis Life Technologies and its products, visit the company’s Web site
at www.synovislife.com.
Forward-looking statements contained in this press release are made
pursuant to the safe harbor provisions of the Private Securities
Litigation Reform Act of 1995. The statements can be identified by words
such as “should”, “could”, “may”, “will”, “expect”, “believe”,
“anticipate”, “estimate”, “continue”, or other similar expressions.
Certain important factors that could cause results to differ materially
from those anticipated by the forward-looking statements made herein
include the timing of product introductions, the ability of our direct
sales force to grow revenues, outcomes of clinical and market trials as
well as regulatory submissions, the number of certain surgical
procedures performed, the ability to identify, acquire and successfully
integrate suitable acquisition candidates, the cost and outcome of
intellectual property litigation, any operational or financial impact of
the current global economic downturn, current market conditions
affecting its investments and any claims for indemnification related to
the sale of the interventional business, as well as the other factors
found in the company’s Annual Report on Form 10-K for the year ended
October 31, 2008.
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SYNOVIS LIFE TECHNOLOGIES, INC.
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|
Condensed Consolidated Results of Operations (unaudited)
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(In thousands, except per share data)
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|
|
|
|
|
|
|
Three Months Ended
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|
|
|
January 31
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|
|
|
2009
|
|
2008
|
|
|
|
|
|
|
|
Net revenue
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|
$
|
13,414
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|
$
|
11,306
|
|
Cost of revenue
|
|
|
3,973
|
|
|
3,685
|
|
Gross margin
|
|
|
9,441
|
|
|
7,621
|
|
Gross margin percentage
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|
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70%
|
|
|
67%
|
|
|
|
|
|
|
|
Selling, general and administrative
|
|
|
6,347
|
|
|
5,655
|
|
Research and development
|
|
|
854
|
|
|
683
|
|
|
|
|
|
|
|
Operating income
|
|
|
2,240
|
|
|
1,283
|
|
|
|
|
|
|
|
Interest income
|
|
|
339
|
|
|
585
|
|
Income from continuing operations before provision for income taxes
|
|
|
2,579
|
|
|
1,868
|
|
Provision for income taxes
|
|
|
916
|
|
|
673
|
|
|
|
|
|
|
|
Income from continuing operations
|
|
|
1,663
|
|
|
1,195
|
|
|
|
|
|
|
|
Discontinued operations:
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|
|
|
|
|
Loss from operations of discontinued business, net of tax benefit
of $10
|
|
|
---
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|
|
(20)
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|
|
|
|
|
|
|
|
|
Gain on sale of discontinued operations, net of taxes of $6,083
|
|
|
---
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|
|
5,340
|
|
|
|
|
|
|
|
Net income
|
|
$
|
1,663
|
|
$
|
6,515
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|
|
|
|
|
|
|
|
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Basic earnings per share:
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|
|
|
|
|
- Continuing operations
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$
|
0.14
|
|
$
|
0.10
|
|
- Discontinued operations
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|
|
---
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|
|
0.43
|
|
Basic earnings per share
|
|
$
|
0.14
|
|
$
|
0.53
|
|
|
|
|
|
|
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Diluted earnings per share:
|
|
|
|
|
|
- Continuing operations
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|
$
|
0.14
|
|
$
|
0.09
|
|
- Discontinued operations
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|
|
---
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|
|
0.42
|
|
Diluted earnings per share
|
|
$
|
0.14
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|
$
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0.51
|
|
|
|
|
|
|
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Weighted average basic shares outstanding
|
|
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11,721
|
|
|
12,373
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|
Weighted average diluted shares outstanding
|
|
|
11,966
|
|
|
12,762
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SYNOVIS LIFE TECHNOLOGIES, INC.
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|
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Condensed Consolidated Balance Sheets
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As of January 31, 2009 (unaudited) and October 31, 2008
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(In thousands, except share and per share data)
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|
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January 31, 2009
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October 31, 2008
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ASSETS
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Current assets:
|
|
|
|
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Cash and cash equivalents
|
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$
|
28,994
|
|
|
$
|
46,895
|
|
|
Restricted cash
|
|
|
2,950
|
|
|
|
2,950
|
|
|
Short-term investments
|
|
|
16,106
|
|
|
|
5,598
|
|
|
Accounts receivable, net
|
|
|
6,163
|
|
|
|
6,071
|
|
|
Inventories
|
|
|
5,670
|
|
|
|
5,733
|
|
|
Other current assets
|
|
|
1,635
|
|
|
|
2,390
|
|
|
Total current assets
|
|
|
61,518
|
|
|
|
69,637
|
|
|
|
|
|
|
|
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Investments, net
|
|
|
17,047
|
|
|
|
19,345
|
|
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Property, plant and equipment, net
|
|
|
2,970
|
|
|
|
2,931
|
|
|
Goodwill and other intangible assets, net
|
|
|
5,125
|
|
|
|
5,158
|
|
|
Deferred income tax asset, net
|
|
|
437
|
|
|
|
330
|
|
|
|
|
|
|
|
|
Total assets
|
|
$
|
87,097
|
|
|
$
|
97,401
|
|
|
|
|
|
|
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LIABILITIES AND SHAREHOLDERS’ EQUITY
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|
|
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Current liabilities:
|
|
|
|
|
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Accounts payable and accrued expenses
|
|
$
|
4,104
|
|
|
$
|
7,168
|
|
|
Deferred income tax liability, net
|
|
|
147
|
|
|
|
147
|
|
|
Current liabilities – discontinued operations
|
|
|
205
|
|
|
|
225
|
|
|
Total current liabilities
|
|
|
4,456
|
|
|
|
7,540
|
|
|
|
|
|
|
|
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Shareholders’ equity:
|
|
|
|
|
|
Preferred stock: authorized 5,000,000 shares of $.01 par
value; none issued or outstanding at both dates
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|
|
---
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|
|
|
---
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Common stock: authorized 20,000,000 shares of $.01 par
value; issued and outstanding 11,530,882 at January 31, 2009
and 12,018,670 at October 31, 2008
|
|
|
115
|
|
|
|
120
|
|
|
Additional paid-in capital
|
|
|
64,341
|
|
|
|
72,181
|
|
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Accumulated other comprehensive loss
|
|
|
(3,445
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)
|
|
|
(2,407
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)
|
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Retained earnings
|
|
|
21,630
|
|
|
|
19,967
|
|
|
Total shareholders’ equity
|
|
|
82,641
|
|
|
|
89,861
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|
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Total liabilities and shareholders’ equity
|
|
$
|
87,097
|
|
|
$
|
97,401
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Source: Synovis Life Technologies, Inc.
Padilla Speer Beardsley Inc. Nancy A. Johnson, 612-455-1745 or Marian
Briggs, 612-455-1742 or Synovis Life Technologies, Inc. Richard
Kramp, President and CEO, 651-796-7300 or Brett Reynolds, CFO,
651-796-7300
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