Seastar Medical Holding Corp (ICU) Stock Price & Analysis
Seastar Medical Holding Corp (ICU) rose 3.11% to USD 2.98 as of September 8, 2026 at 13:17 UTC, according to Nexqual real-time market data.
ICU last closed at USD 2.98; the session ranged USD 2.84–3.01 on volume of 25,261 shares. Market capitalization is —, with a 52-week range of USD 2.07–12.5 (NCM). Source: Nexqual, September 8, 2026 at 13:17 UTC.
Key Statistics (as of September 8, 2026 at 13:17 UTC)
| Price | USD 2.98 |
|---|---|
| Change | ▲ 3.11% (up) |
| Previous Close | USD 2.98 |
| Open | USD 2.98 |
| Day Range | USD 2.84 – 3.01 |
| 52-Week Range | USD 2.07 – 12.5 |
| Volume | 25,261 shares |
| Market Cap | — |
| Exchange | NCM |
Technical Analysis (ICU)
Nexqual's technical model rates ICU "STRONG SELL" based on 0 bullish and 5 bearish signals across 128 daily candles, as of September 8, 2026 at 13:17 UTC.
| Overall Signal | STRONG SELL |
|---|---|
| RSI (14) | 35.29 (neutral) |
| vs SMA50 | Below (USD 3.66) |
| MACD | -0.16 (negative) |
From Seastar Medical Holding Corp's Latest SEC 10-K Filing (filed 2026-03-25)
Key Strengths & Strategy (as disclosed to the SEC)
- Our success depends in large part on our ability to protect our proprietary technology, including our SCD technologies, and to operate without infringing the proprietary rights of third parties.   17 Table of Contents   The term of individual patents depends on the legal term of the patents in the countries in which they are obtained.
- In consideration for such exclusive license, during the term of the UOM License Agreement, we agreed to pay the UOM a royalty fee equal to 1% of net sales as well as a one-time milestone payment of $0.1 million upon FDA approval of the first licensed product under the license (paid in 2024), and to reimburse patent costs.
- On February 21, 2024, we announced a final Approval Order for the HDE, which allows us to commercialize QUELIMMUNE.   Clinical Progression   NEUTRALIZE-AKI Design   We are actively enrolling and treating patients in a pivotal clinical trial of the SCD for the treatment of AKI in adults, an indication awarded BDD by the FDA in April 2022.
- We also rely on know-how, confidentiality agreements, license agreements and other agreements to establish and protect our proprietary rights.
Partnerships
- In addition to the Supply Agreement with FUSA, we are developing a second source for both adult and pediatric cartridges, which will enable us to better manage potential supply disruptions.   Additionally, use of the SCD in hospital settings requires the administration of RCA and calcium replacement into CRRT circuitry for safe and effective use.
- If during such period, we elect to promote and sell the SCD through distributors, we will be required to provide FUSA with a right of first refusal to be our exclusive distributor of the SCD in the United States and its territories, provided that the SCD is not promoted or sold in a manner that is incompatible with any devices manufactured and/or sold by FUSA or its affiliates.   On December 27, 2022, we entered into a license and distribution agreement with Nuwellis.
Source: SEC EDGAR 10-K, official filing. Curated by Nexqual.
Peers & Related Stocks
| Symbol | Name | Price | Change |
|---|---|---|---|
| CDIO | Cardio Diagnostics Holdings Inc | USD 1.86 | ▲ 1.09% |
| ZVSA | ZyVersa Therapeutics, Inc. | USD 0.1 | ▲ 4.04% |
| FEMY | Femasys Inc. | USD 2.98 | ▼ 3.87% |
| AVTX | Avalo Therapeutics, Inc. | USD 19.23 | ▼ 0.57% |
| RNAZ | TransCode Therapeutics, Inc. | USD 2.06 | ▲ 2.49% |
Data source: Nexqual — real-time market data, technical indicators, analyst consensus, earnings, SEC EDGAR filings. Last updated: September 8, 2026 at 13:17 UTC. This page is informational and not investment advice.