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Emblok

2 viewers · 30d

Total raised

$6.0M

+$6.0M this year

1 filing since 2026 · latest Equity filed

Cumulative raised
LAST ROUND
Equity · $6.0M
ROUNDS
1
INVESTORS
1
FOUNDED
2025
HQ
Tampa, FL
SECTOR
Healthcare
EMPLOYEES
N/A
30D VIEWERS
2

AI overview

Updated

Emblok, Inc. is a privately held Tampa, Florida medical device company developing the Emblok Embolic Protection System, a 360-degree whole-body embolic protection device used during transcatheter aortic valve replacement (TAVR). The device is delivered through femoral access, deployed across the aortic arch near the brachiocephalic artery, and captures calcium and tissue debris dislodged during valve replacement before it can reach the brain, kidneys, or visceral arteries. The company was formerly known as Innovative Cardiovascular Solutions. The system is investigational and its clinical use is limited to an FDA-approved study; a US multicenter randomized trial enrolling up to 532 TAVR patients is underway, having passed 50 patients enrolled in October 2024.

What sets it apart

Where most cerebral embolic protection devices filter only the vessels feeding the brain, Emblok is designed as whole-body protection, capturing debris across all major arteries to also address acute kidney injury and peripheral vascular complications from TAVR.

Funding history

1 round
Equity+1May 21, 2026
Form D
+$6.0M$6.0M total

Latest SEC filings

via EDGAR · CIK 0002140377
Form D · May 21, 2026NewView on EDGAR

Products

1 tracked

Emblok Embolic Protection System (EPS)

Interventional cardiology device

A catheter-delivered 360-degree whole-body embolic protection filter deployed in the aortic arch during TAVR, which captures embolic debris while maintaining blood flow and is then re-sheathed and withdrawn via femoral access.

  • 360-degree whole-body coverage rather than cerebral-only filtration
  • Single femoral access delivery, deployment, capture, and retrieval workflow
  • Filter seats against vessel walls for full coverage while preserving blood flow
  • Under evaluation in a US multicenter randomized trial of up to 532 TAVR patients (NCT07129421)