Lucid Diagnostics (NASDAQ:LUCD – Get Free Report) and enVVeno Medical (NASDAQ:NVNO – Get Free Report) are both small-cap medical companies, but which is the better business? We will compare the two businesses based on the strength of their valuation, earnings, profitability, dividends, risk, institutional ownership and analyst recommendations.
Profitability
This table compares Lucid Diagnostics and enVVeno Medical’s net margins, return on equity and return on assets.
Net Margins | Return on Equity | Return on Assets | |
Lucid Diagnostics | -1,227.74% | N/A | -112.67% |
enVVeno Medical | N/A | -54.24% | -50.69% |
Valuation & Earnings
This table compares Lucid Diagnostics and enVVeno Medical”s gross revenue, earnings per share (EPS) and valuation.
Gross Revenue | Price/Sales Ratio | Net Income | Earnings Per Share | Price/Earnings Ratio | |
Lucid Diagnostics | $3.80 million | 10.81 | -$52.67 million | ($1.27) | -0.62 |
enVVeno Medical | N/A | N/A | -$23.52 million | ($1.66) | -1.88 |
Institutional & Insider Ownership
74.0% of Lucid Diagnostics shares are held by institutional investors. Comparatively, 34.7% of enVVeno Medical shares are held by institutional investors. 8.8% of Lucid Diagnostics shares are held by company insiders. Comparatively, 17.0% of enVVeno Medical shares are held by company insiders. Strong institutional ownership is an indication that large money managers, endowments and hedge funds believe a stock is poised for long-term growth.
Analyst Recommendations
This is a breakdown of recent ratings for Lucid Diagnostics and enVVeno Medical, as provided by MarketBeat.
Sell Ratings | Hold Ratings | Buy Ratings | Strong Buy Ratings | Rating Score | |
Lucid Diagnostics | 0 | 0 | 4 | 1 | 3.20 |
enVVeno Medical | 0 | 0 | 0 | 0 | N/A |
Lucid Diagnostics currently has a consensus target price of $3.94, indicating a potential upside of 402.36%. Given Lucid Diagnostics’ higher possible upside, equities analysts plainly believe Lucid Diagnostics is more favorable than enVVeno Medical.
Risk and Volatility
Lucid Diagnostics has a beta of 1.47, meaning that its share price is 47% more volatile than the S&P 500. Comparatively, enVVeno Medical has a beta of 1.21, meaning that its share price is 21% more volatile than the S&P 500.
Summary
Lucid Diagnostics beats enVVeno Medical on 9 of the 13 factors compared between the two stocks.
About Lucid Diagnostics
Lucid Diagnostics Inc. operates as a commercial-stage medical diagnostics technology company in the United States. The company focuses on patients with gastroesophageal reflux disease (GERD) who are at risk of developing esophageal precancer and cancer, primarily highly lethal esophageal adenocarcinoma. Its flagship product, the EsoGuard Esophageal DNA Test performed on samples collected with the EsoCheck Esophageal Cell collection device, a testing tool with the goal of preventing EAC deaths through early detection of esophageal precancer in at-risk GERD patients. The company was incorporated in 2018 and is based in New York, New York. Lucid Diagnostics Inc. is a subsidiary of PAVmed Inc.
About enVVeno Medical
enVVeno Medical Corporation (Nasdaq: NVNO) is an medical device company focused on the development of innovative bioprosthetic (tissue-based) devices to improve the standard of care in the treatment of venous disease. The company’s lead product, the VenoValve®️, is a first-in-class, surgical implant being developed for the treatment of severe deep venous Chronic Venous Insufficiency (CVI). Deep venous CVI occurs when valves inside of the deep veins of the leg become damaged, resulting in insufficient blood being returned to the heart. The malfunctioning vein valves cause blood to flow backwards (reflux) and pool in the lower leg, increasing the pressure within the veins of the leg (venous hypertension). In the most severe cases, CVI can lead to venous ulcers (open skin sores) that become chronic and difficult to heal. The VenoValve is implanted in the femoral vein and works as a replacement venous valve, designed to reduce reflux and venous hypertension, and to restore proper directional blood flow back to the heart. With severe deep venous CVI impacting an estimated 2.4 million people in the U.S., who have no effective treatment options, the VenoValve has received Breakthrough Device Designation from the U.S. Food and Drug Administration, and is currently being evaluated in the SAVVE U.S. clinical trial.
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