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AORT Overview

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$
0.000
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0.000(0.000%)Aft-market
ET
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0.000
0.000(0.000%)
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0.000(0.000%)Aft-market
ET
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Intellectia

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High
37.350
Open
37.190
VWAP
36.87
Vol
265.25K
Mkt Cap
1.78B
Low
36.510
Amount
9.78M
EV/EBITDA(TTM)
40.05
Total Shares
48.50M
EV
1.97B
EV/OCF(TTM)
49.42
P/S(TTM)
3.97
Artivion, Inc. is engaged in manufacturing, processing, and distribution of medical devices and implantable human tissues used in cardiac and vascular surgical procedures for patients with aortic disease. The Company operates through two segments, which include Medical Devices and Preservation Services. The medical devices and preservation services are primarily used by cardiac and vascular surgeons to treat patients with aortic disease, including heart valve disease, aortic aneurysms, and dissections, and, to a lesser extent, other conditions in cardiac and vascular surgery. It has four product families: aortic stent grafts, On-X mechanical heart valves and related surgical products, surgical sealants, and implantable cardiac and vascular human tissues. Its aortic stent grafts include aortic arch stent grafts, abdominal stent grafts, and synthetic vascular grafts. Its surgical sealants include BioGlue Surgical Adhesive products.
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Events Timeline

(ET)
2026-04-07
07:10:00
Artivion Receives FDA Approval for Nexus Aortic Arch System
select
2026-02-12 (ET)
2026-02-12
16:10:00
Sees 2026 Adjusted EBITDA of $105M-$110M
select
2026-02-12
16:10:00
Company Reports Q4 Revenue of $116M, Below Expectations
select
2026-02-02 (ET)
2026-02-02
08:11:00
Artivion Presents New Clinical Data at Annual Thoracic Surgeons Meeting
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News

Yahoo Finance
6.5
04-13Yahoo Finance
Analysis of Stocks Under $50
  • Risks of Box: Box (NYSE: BOX) is currently priced at $21.46, and despite its role as a 'Content Cloud' managing 90% of unstructured business data, its average billings growth of 11.9% raises concerns about future demand stability.
  • Challenges for Artivion: Artivion (NYSE: AORT) trades at $37.63, and while it operates in the cardiac and vascular device market, its revenue of $441.3 million indicates limited distribution channels, and the lack of free cash flow hampers its reinvestment capabilities.
  • Growth Potential of WisdomTree: WisdomTree (NYSE: WT) is priced at $15.84, and with an impressive annual revenue growth of 18.9% and a 52.5% increase in earnings per share, it demonstrates strong market share gains and is expected to continue outperforming the market.
  • Stocks to Watch: In the current market environment, investors should focus on stocks that not only have strong fundamentals but are also experiencing upward momentum to seize potential investment opportunities.
NASDAQ.COM
9.5
04-08NASDAQ.COM
Artivion Shares Surge 5.3% on FDA Approval News
  • Stock Price Surge: Artivion's shares rose 5.3% in the last trading session to close at $35.22, with trading volume significantly exceeding normal levels, reflecting investor optimism about the company's prospects.
  • FDA Approval Impact: The FDA's premarket approval for the NEXUS Aortic Arch System allows Artivion to exercise its option to acquire its long-standing partner Endospan within 90 days of receiving this notice, further strengthening the company's market position.
  • Earnings Expectations: Artivion is expected to report quarterly earnings of $0.06 per share, unchanged from the year-ago quarter, with revenues projected at $115.95 million, representing a 17.1% increase, indicating growth potential in the medical device sector.
  • Market Trend Monitoring: Although the current EPS estimate has remained unchanged over the past 30 days, research shows that trends in earnings estimate revisions are closely correlated with short-term stock price movements, prompting investors to monitor Artivion's future performance closely.
NASDAQ.COM
8.5
04-07NASDAQ.COM
Artivion Receives FDA Approval for NEXUS Aortic Arch System
  • FDA Approval Milestone: Artivion announced that its NEXUS Aortic Arch System has received premarket approval from the U.S. FDA, becoming the first branched endovascular stent graft cleared for use, offering a safer alternative to open-chest surgery and marking a significant advancement in the treatment of complex aortic arch disease.
  • Clinical Data Support: The NEXUS TRIOMPHE IDE trial demonstrated that 90% of patients avoided lesion-related death, 90% were free from disabling stroke, and 98% avoided reintervention due to endoleaks one year post-treatment, highlighting the clinical value of this technology in a high-risk patient population.
  • Global Market Expansion: The FDA approval allows Artivion to promote the NEXUS system in the U.S. market, further enhancing its influence in the global cardiovascular solutions sector while providing broader treatment options for American patients.
  • Acquisition Opportunity: The FDA approval entitles Artivion to acquire Endospan Ltd. within 90 days, supported by a $150 million delayed draw term loan, reflecting the company's proactive strategy in investment and market expansion.
NASDAQ.COM
8.5
04-07NASDAQ.COM
Artivion Receives FDA Approval for NEXUS System
  • FDA Approval: Artivion's NEXUS Aortic Arch System has received FDA approval, marking a significant advancement in the minimally invasive treatment of aortic arch disease, which is expected to enhance the company's competitiveness in this market.
  • Acquisition Option: Following the FDA approval, Artivion has a 90-day window to exercise its option to acquire its partner Endospan, reflecting the company's proactive stance towards future growth opportunities that could strengthen its product portfolio.
  • Funding Preparedness: Artivion has a $150 million delayed-draw term loan in place to support a potential acquisition, providing the company with financial flexibility to ensure it is not constrained during the acquisition process.
  • Clinical Data Support: The FDA approval of the NEXUS system is backed by data from the NEXUS TRIOMPHE IDE trial, which demonstrated a 90% survival rate and a 98% freedom from reintervention in a high-risk patient population, further validating the product's clinical efficacy and market potential.
PRnewswire
8.5
04-07PRnewswire
Endospan's NEXUS Stent Graft System Approved by FDA for Aortic Arch Disease
  • FDA Approval Milestone: Endospan's NEXUS stent graft system has received premarket approval from the FDA, representing a significant breakthrough in treatment options for aortic arch diseases, including chronic aortic dissections, which is expected to greatly enhance patient survival rates and quality of life.
  • Acquisition Option Activation: Artivion can exercise its option to acquire Endospan within 90 days of FDA approval, reflecting the company's confidence in future market potential, and has secured a $150 million loan to support this potential acquisition.
  • Clinical Data Validation: The NEXUS system demonstrated a 90% patient survival rate, 90% freedom from disabling stroke, and 98% freedom from reintervention due to endoleaks at one year in the TRIOMPHE IDE trial, underscoring its effectiveness and safety in high-risk patient populations.
  • Expansive Market Outlook: The approval of NEXUS opens new opportunities for Artivion's market expansion across over 100 countries, particularly in the aortic disease treatment sector, which is anticipated to drive future revenue growth and increase market share.
Newsfilter
8.5
04-07Newsfilter
Endospan's NEXUS Stent Graft System Receives FDA Approval
  • FDA Approval Milestone: Endospan's NEXUS stent graft system has received premarket approval from the FDA, marking a significant advancement in the treatment options for aortic arch diseases, including chronic aortic dissections, which is expected to greatly enhance patient survival rates and treatment accessibility.
  • Acquisition Option Activation: Artivion has the option to acquire Endospan within 90 days of FDA approval and has secured a $150 million delayed draw term loan, indicating the company's proactive financial strategy and readiness for potential integration.
  • Clinical Data Validation: The NEXUS system demonstrated impressive outcomes in the TRIOMPHE IDE trial, with 90% patient survival at one year, 90% freedom from disabling stroke, and 98% freedom from reintervention due to endoleaks, underscoring its clinical efficacy in a high-risk patient population.
  • Significant Market Potential: The introduction of the NEXUS system provides a new treatment avenue for patients with aortic arch disease, who have historically faced limited options, and with Artivion's presence in over 100 countries, this is expected to drive further global market expansion.
Wall Street analysts forecast AORT stock price to rise
7 Analyst Rating
Wall Street analysts forecast AORT stock price to rise
6 Buy
1 Hold
0 Sell
Strong Buy
Current: 0.000
sliders
Low
40.00
Averages
51.71
High
58.00
Current: 0.000
sliders
Low
40.00
Averages
51.71
High
58.00
Ladenburg
Jeffrey Cohen
Neutral -> Buy
upgrade
$42
AI Analysis
2026-04-10
Reason
Ladenburg
Jeffrey Cohen
Price Target
$42
AI Analysis
2026-04-10
upgrade
Neutral -> Buy
Reason
Ladenburg analyst Jeffrey Cohen upgraded Artivion to Buy from Neutral with a $42 price target.
Canaccord
William Plovanic
Buy
downgrade
$51 -> $48
2026-02-13
Reason
Canaccord
William Plovanic
Price Target
$51 -> $48
2026-02-13
downgrade
Buy
Reason
Canaccord analyst William Plovanic lowered the firm's price target on Artivion to $48 from $51 and keeps a Buy rating on the shares. The firm said Artivion reported a very strong Q4 that was somewhat masked by a one-time revenue reduction to settle a $2.3M payment to the Italian government. Management issued guidance at the midpoint which contemplates low 20% growth in aortic stent grafts, mid-teens growth in On-X, MSD growth in BioGlue and no growth in tissue services.
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Valuation Metrics

The current forward P/E ratio for Artivion Inc (AORT.N) is 60.98, compared to its 5-year average forward P/E of 85.33. For a more detailed relative valuation and DCF analysis to assess Artivion Inc's fair value, Click here.

Forward PE

The forward P/E ratio is a valuation metric that divides a company's current stock price by its estimated future earnings per share over the next 12 months.
StronglyUndervaluedUndervaluedFairOvervaluedStronglyOvervalueddotted line Image
N/A
5Y Average PE
85.33
Current PE
60.98
Overvalued PE
1246.43
Undervalued PE
-1075.77

Forward EV/EBITDA

The forward EV/EBITDA ratio is a valuation metric that divides a company's enterprise value (EV) by its estimated future earnings before interest, taxes, depreciation, and amortization (EBITDA) over the next 12 months.
StronglyUndervaluedUndervaluedFairOvervaluedStronglyOvervalueddotted line Image
5Y Average EV/EBITDA
21.13
Current EV/EBITDA
30.55
Overvalued EV/EBITDA
26.99
Undervalued EV/EBITDA
15.27

Forward PS

The forward P/S ratio is a valuation metric that divides a company's current stock price by its estimated future sales (or revenue) per share over the next 12 months.
StronglyUndervaluedUndervaluedFairOvervaluedStronglyOvervalueddotted line Image
5Y Average PS
2.59
Current PS
3.31
Overvalued PS
3.41
Undervalued PS
1.77

Financials

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Whales Holding AORT

S
Summit Partners Public Asset Management, LLC
Holding
AORT
+24.81%
3M Return
P
Perceptive Advisors LLC
Holding
AORT
+12.83%
3M Return
N
Next Century Growth Investors LLC
Holding
AORT
-0.81%
3M Return
P
Peregrine Capital Management, LLC
Holding
AORT
-8.79%
3M Return

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Frequently Asked Questions

What is Artivion Inc (AORT) stock price today?

The current price of AORT is 36.74 USD — it has decreased -1.95

What is Artivion Inc (AORT)'s business?

Artivion, Inc. is engaged in manufacturing, processing, and distribution of medical devices and implantable human tissues used in cardiac and vascular surgical procedures for patients with aortic disease. The Company operates through two segments, which include Medical Devices and Preservation Services. The medical devices and preservation services are primarily used by cardiac and vascular surgeons to treat patients with aortic disease, including heart valve disease, aortic aneurysms, and dissections, and, to a lesser extent, other conditions in cardiac and vascular surgery. It has four product families: aortic stent grafts, On-X mechanical heart valves and related surgical products, surgical sealants, and implantable cardiac and vascular human tissues. Its aortic stent grafts include aortic arch stent grafts, abdominal stent grafts, and synthetic vascular grafts. Its surgical sealants include BioGlue Surgical Adhesive products.

What is the price predicton of AORT Stock?

Wall Street analysts forecast AORT stock price to rise over the next 12 months. According to Wall Street analysts, the average 1-year price target for AORT is51.71 USD with a low forecast of 40.00 USD and a high forecast of 58.00 USD. However, analyst price targets are subjective and often lag stock prices, so investors should focus on the objective reasons behind analyst rating changes, which better reflect the company's fundamentals.

What is Artivion Inc (AORT)'s revenue for the last quarter?

Artivion Inc revenue for the last quarter amounts to 115.99M USD, increased 19.20

What is Artivion Inc (AORT)'s earnings per share (EPS) for the last quarter?

Artivion Inc. EPS for the last quarter amounts to 0.05 USD, decreased -112.82

How many employees does Artivion Inc (AORT). have?

Artivion Inc (AORT) has 1800 emplpoyees as of April 17 2026.

What is Artivion Inc (AORT) market cap?

Today AORT has the market capitalization of 1.78B USD.