| Breakdown | TTM | Dec 2024 | Dec 2023 | Dec 2022 | Dec 2020 | Dec 2019 |
|---|---|---|---|---|---|---|
Income Statement | ||||||
| Total Revenue | 51.69M | 59.81M | 27.81M | 7.63M | 0.00 | 0.00 |
| Gross Profit | 23.03M | 24.21M | 362.00K | -10.65M | 0.00 | 0.00 |
| EBITDA | -94.36M | -97.98M | -76.31M | -73.74M | -32.33M | -28.84M |
| Net Income | -99.39M | -113.81M | -94.12M | -84.24M | -34.10M | -29.47M |
Balance Sheet | ||||||
| Total Assets | 266.30M | 295.74M | 45.95M | 38.66M | 30.52M | 7.87M |
| Cash, Cash Equivalents and Short-Term Investments | 201.21M | 237.59M | 8.25M | 14.81M | 24.34M | 5.76M |
| Total Debt | 3.10M | 44.31M | 45.17M | 39.13M | 22.85M | 452.00K |
| Total Liabilities | 82.14M | 90.34M | 255.33M | 156.23M | 28.76M | 4.02M |
| Stockholders Equity | 184.16M | 205.41M | -209.38M | -117.58M | 1.77M | 3.86M |
Cash Flow | ||||||
| Free Cash Flow | -88.63M | -101.20M | -84.75M | -85.10M | -30.23M | -30.52M |
| Operating Cash Flow | -68.36M | -77.61M | -72.23M | -69.64M | -29.89M | -30.29M |
| Investing Cash Flow | -20.06M | -23.31M | -12.23M | -15.46M | -334.00K | -232.00K |
| Financing Cash Flow | 212.71M | 330.26M | 77.72M | 96.11M | 48.81M | 30.24M |
Name | Overall Rating | Market Cap | P/E Ratio | ROE | Dividend Yield | Revenue Growth | EPS Growth |
|---|---|---|---|---|---|---|---|
61 Neutral | $492.34M | ― | -17.10% | ― | 2.73% | 87.03% | |
56 Neutral | $1.23B | ― | -5.20% | ― | -18.82% | 92.56% | |
52 Neutral | $1.38B | ― | ― | ― | 83.78% | -25.37% | |
51 Neutral | $7.86B | -0.30 | -43.30% | 2.27% | 22.53% | -2.21% | |
48 Neutral | $178.62M | -3.07 | -15.30% | ― | -43.95% | -620.21% | |
47 Neutral | $1.26B | ― | -24.65% | ― | -32.42% | -540.37% | |
44 Neutral | $899.28M | ― | -86.99% | ― | ― | -40.63% |
On December 4, 2025, Kestra Medical Technologies, Ltd. successfully closed an underwritten public offering of 6,900,000 common shares, raising approximately $148.4 million. The proceeds are intended to support sales, marketing, commercialization, research and development, clinical studies, and general corporate purposes.
On November 10, 2025, Kestra Medical Technologies announced the results of the ASSURE WCD Clinical Evaluation Post-Approval Study (ACE-PAS) at the American Heart Association Scientific Sessions in New Orleans. The study, which is the largest real-world examination of wearable defibrillators to date, confirmed the strong safety and effectiveness of Kestra’s ASSURE device in clinical practice. Key findings included a 100% success rate in converting ventricular tachycardia and fibrillation events, a low inappropriate-shock rate, and high patient compliance. These results underscore the critical role of wearable defibrillators in protecting patients at risk of sudden cardiac death, potentially informing future clinical practices.