| Breakdown | TTM | Dec 2024 | Dec 2023 | Dec 2022 | Dec 2021 | Dec 2020 |
|---|---|---|---|---|---|---|
Income Statement | ||||||
| Total Revenue | 464.99M | 482.04M | 433.14M | 450.89M | 467.36M | 338.30M |
| Gross Profit | 346.34M | 366.30M | 326.66M | 345.87M | 353.16M | 250.98M |
| EBITDA | 19.75M | 15.76M | 36.03M | 40.32M | 87.00M | 37.23M |
| Net Income | 1.00M | 861.00K | 4.95M | 15.53M | 94.20M | 17.23M |
Balance Sheet | ||||||
| Total Assets | 509.83M | 497.89M | 460.02M | 449.36M | 443.26M | 290.22M |
| Cash, Cash Equivalents and Short-Term Investments | 64.37M | 135.57M | 104.34M | 102.48M | 113.93M | 84.39M |
| Total Debt | 40.81M | 43.31M | 119.35M | 123.79M | 132.30M | 84.77M |
| Total Liabilities | 123.85M | 112.57M | 181.36M | 183.69M | 201.92M | 148.41M |
| Stockholders Equity | 385.98M | 385.32M | 278.66M | 265.67M | 241.34M | 141.81M |
Cash Flow | ||||||
| Free Cash Flow | -51.65M | 4.18M | 6.55M | -9.04M | 30.76M | -12.21M |
| Operating Cash Flow | -38.79M | 14.21M | 30.92M | 24.86M | 61.98M | 5.47M |
| Investing Cash Flow | -12.86M | -10.03M | -24.36M | -33.90M | -31.22M | -23.50M |
| Financing Cash Flow | 21.10M | 27.64M | -5.50M | -2.20M | -1.04M | 42.47M |
Name | Overall Rating | Market Cap | P/E Ratio | ROE | Dividend Yield | Revenue Growth | EPS Growth |
|---|---|---|---|---|---|---|---|
73 Outperform | $447.57M | 5.99 | 39.94% | ― | -0.85% | -13.50% | |
71 Outperform | $672.78M | 9.69 | 13.92% | ― | -29.91% | ― | |
56 Neutral | $965.82M | -7.24 | ― | ― | 2.83% | 13.61% | |
51 Neutral | $7.86B | -0.30 | -43.30% | 2.27% | 22.53% | -2.21% | |
50 Neutral | $724.67M | -58.61 | 0.30% | ― | 2.24% | -67.56% | |
50 Neutral | $466.05M | -7.46 | ― | ― | 15.10% | 0.18% | |
48 Neutral | $460.92M | -7.07 | -7.82% | ― | 1.76% | 18.31% |
On September 25, 2025, Organogenesis Holdings announced that its second Phase 3 trial of ReNu, a cryopreserved amniotic suspension allograft for knee osteoarthritis, did not achieve statistical significance for its primary endpoint. Despite this, the trial showed a numerical improvement in baseline pain reduction and maintained a favorable safety profile. The company plans to request a pre-Biologics License Application meeting with the FDA to discuss using combined data from both Phase 3 studies to support a BLA approval, emphasizing ReNu’s potential to address unmet medical needs in knee osteoarthritis.