$BCDA

BioCardia, Inc.

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$4K
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Altman Peter
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Altman Peter purchased $475 of BCDA

Altman Peter (President and CEO) purchased 500 shares of BioCardia, Inc. (BCDA) at $0.95 across 2 trades over 2026-10-15 to 2026-10-16.

BioCardia: FDA Accepts De Novo Pre-Submission for Helix Catheter; Substantive Review, Meeting Expected This Quarter

BioCardia's FDA pre-submission for Helix catheter was accepted, with substantive review and a meeting expected this quarter. The FDA raised no concerns about safety or performance. The company has clinical data from 15 trials supporting potential clearance, which could expand partnerships. According to the company, marketing clearance could enhance opportunities with cardiac biologics developers.

BioCardia Announces FDA Acceptance of De Novo Pre-Submission Package for HelixTM Catheter Marketing Clearance FDA Substantive Review and Meeting Expected…

BioCardia, Inc. (BCDA) filed an SEC Form 8-K — Other Events. Exhibit 99.1 BioCardia Announces FDA Acceptance of De Novo Pre-Submission Package for Helix TM Catheter Marketing Clearance FDA Substantive Review and Meeting Expected this Quarter October 19, 2026, Sunnyvale, Calif. BioCardia, Inc. [NASDAQ: BCDA] , a global leader in cellular an

BCDA sentiment & insider activity

Over the past 7 days, AlphAI's AI scored 6 news stories mentioning BCDA (BioCardia, Inc.). Coverage has skewed bullish: 6 bullish, 0 neutral, and 0 bearish.

Recent BCDA coverage spans regulation, insider activity and financial news.

In the last 30 days, BCDA insiders filed 4 SEC Form 4 transactions — 4 purchases ($4K) and no sales. The most active reporter was Altman Peter, President and CEO, with 4 filings.

What's driving BCDA

AlphAI scores every news story that mentions BCDA with an AI model for sentiment and relevance, and aggregates insider trades from BioCardia, Inc.'s SEC EDGAR Form 4 filings. Figures refresh continuously.

News on $BCDA

Score
$BCDAHighAI 8/10

BioCardia: FDA Accepts De Novo Pre-Submission for Helix Catheter; Substantive Review, Meeting Expected This Quarter

BioCardia's FDA pre-submission for Helix catheter was accepted, with substantive review and a meeting expected this quarter. The FDA raised no concerns about safety or performance. The company has clinical data from 15 trials supporting potential clearance, which could expand partnerships. According to the company, marketing clearance could enhance opportunities with cardiac biologics developers.

$BCDAHighAI 8/10

BioCardia Announces FDA Acceptance of De Novo Pre-Submission Package for HelixTM Catheter Marketing Clearance FDA Substantive Review and Meeting Expected…

BioCardia, Inc. (BCDA) filed an SEC Form 8-K — Other Events. Exhibit 99.1 BioCardia Announces FDA Acceptance of De Novo Pre-Submission Package for Helix TM Catheter Marketing Clearance FDA Substantive Review and Meeting Expected this Quarter October 19, 2026, Sunnyvale, Calif. BioCardia, Inc. [NASDAQ: BCDA] , a global leader in cellular an

$BCDAMedAI 8/10

BioCardia Presents CardiAMP HF II Trial Design at Heart Failure Society of America Annual Scientific Meeting

BioCardia, Inc. (BCDA) filed an SEC Form 8-K — Other Events. Exhibit 99.1 BioCardia Presents CardiAMP HF II Trial Design at Heart Failure Society of America Annual Scientific Meeting SUNNYVALE, Calif. – October 7, 2026 – BioCardia, Inc. [Nasdaq: BCDA], a global leader in cellular and cell-derived therapeutics for the treatment of cardiovas

BioCardia Files Revised De Novo Pre-Submission for FDA Approval of Helix™ Catheter

BioCardia (BCDA) submitted a revised pre-submission to the FDA for approval of its Helix Catheter, following FDA feedback. The FDA previously agreed on two pathways for marketing clearance and had no concerns about safety data or device performance. FDA aims to review the submission within 15 days and provide feedback within 70 days. Approval could expand BioCardia's partnership opportunities for targeted heart delivery of therapeutics.

$BCDAMed

BioCardia Confirms Timing and Provides Update on FDA Helix Pre-Submission and PMDA CardiAMP HF Shonin Submission

BioCardia, Inc. (BCDA) filed an SEC Form 8-K — Other Events. Exhibit 99.1 BioCardia Confirms Timing and Provides Update on FDA Helix Pre-Submission and PMDA CardiAMP HF Shonin Submission SUNNYVALE, Calif. – September 23, 2026 – BioCardia, Inc. [Nasdaq: BCDA], a global leader in cellular and cell-derived therapeutics for the treatment of ca

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