Vascular Solutions is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Vascular Solutions - FDA 510(k) Cleared Devices
Recent clearances: Wattson Temporary Pacing Guidewire
1
Total
1
Cleared
0
Denied
Vascular Solutions, specializes in Cardiovascular devices for interventional procedures. The company operates with a manufacturing facility in Maple Grove, US. Now part of Teleflex, the brand continues to operate under the parent company's interventional portfolio.
The company has received 1 FDA 510(k) clearance from 1 total submission. All regulatory activity occurred in 2020, reflecting the company's historical record in the Cardiovascular device space. The cleared device, Wattson Temporary Pacing Guidewire, represents the company's focus on specialized interventional technologies.
Vascular Solutions' product portfolio emphasizes vascular access, closure systems, and temporary pacing solutions for complex catheterization and structural heart procedures. These devices support interventional cardiologists and radiologists in access management and hemostasis control during endovascular procedures.
Explore the company's FDA 510(k) clearance history, device names, product codes, and clearance dates in the regulatory database.
1 device has linked clinical trial registered on ClinicalTrials.gov.
FDA 510(k) Regulatory Record - Vascular Solutions
1 devices