MYNX CONTROL Vascular Closure Device
Extravascular closure designed for procedural control and patient comfort.
The MYNX CONTROL® Vascular Closure Device (VCD) provides reliable arterial access site closure using a bioabsorbable PEG sealant and GRIP TECHNOLOGY®. The system is designed to deliver controlled, extravascular sealing supporting rapid hemostasis and improved patient recovery.
Closing the Femoral Access Site Efficiently and Safely
Femoral access procedures require reliable vascular closure that balances procedural efficiency, patient comfort, and safety. Traditional closure techniques may involve longer recovery times, intravascular implants, or inconsistent hemostasis.
MYNX CONTROL VCD is designed to provide controlled extravascular sealing without leaving anything permanent inside the artery.
A Controlled Approach to Vascular Closure
MYNX CONTROL VCD combines a simple delivery system with GRIP TECHNOLOGY to provide secure extravascular closure.
The device uses a bioabsorbable PEG sealant that expands within the tissue tract to seal the arteriotomy while remaining outside the vessel lumen.
- Two-button deployment system
- Sheath catch for precise positioning
- PEG sealant technology
- Extravascular closure approach
How MYNX CONTROL VCD Achieves Closure
MYNX CONTROL VCD Step-by-Step
This animated overview highlights the key features and mechanism of the MYNX CONTROL Vascular Closure Device, illustrating how the system is designed to support secure and efficient femoral artery closure. Watch to better understand device functionality and procedural benefits in a clear, visual format.
MYNX CONTROL VCD Actual Physician Case
This physician procedure video demonstrates the MYNX CONTROL Vascular Closure Device, highlighting key techniques for effective and reliable femoral artery closure. Gain practical insights to support consistent outcomes and streamline your post-procedural workflow.
GRIP TECHNOLOGY Active Sealing
MYNX CONTROL VCD uses GRIP TECHNOLOGY, a combination of mechanical positioning and PEG sealant expansion that delivers reliable extravascular closure. The hydrophilic polyethylene glycol sealant expands within the tissue tract and forms a seal that mimics the structure of a natural fibrin clot.
Grip Tip
Helps secure positioning at the arteriotomy.
PEG Sealant
Expands and interlocks within the tissue tract.
Extravascular Closure
Leaves nothing permanent behind.
MYNX CONTROL VCD
MYNX Portfolio of Vascular Closure Devices (VCP) Clinical Evidence
Product Characteristics
Scroll, sort or search for the particular MYNX CONTROL Vascular Closure Device's part number of interest.
| SKU | Product Description | Sheath Compatibility (F) | Qty/box | Where Used/Indication |
|---|---|---|---|---|
| MX6760 | MYNX CONTROL Vascular Closure Device 6/7F | 6/7 | 10 | Femoral artery |
| MX5060 | MYNX CONTROL Vascular Closure Device 5F | 5 | 10 | Femoral artery |
References
1. Scheinert D, Sievert H, Turco MA, et al. The safety and efficacy of an extravascular, water‐soluble sealant for vascular closure: Initial clinical results for Mynx. Cathet Cardiovasc Intervent. 2007 Oct;70:627-633.
2 MYNX CONTROL Vascular Closure Device Instructions for Use.
3 Pruski MJ Jr, Blachut AM, Konkolewska M, et al. MynxGrip for closure of antegrade puncture after peripheral interventions with same-day discharge. Vasc Endovasc Surg. 2017 Feb;51(2):67-71.
4 Baker NC, Escarcega RO, Lipinski MJ, et al. Active versus passive anchoring vascular closure devices following percutaneous coronary intervention: a safety and efficacy comparative analysis. J Interv Cardiol. 2016 Feb; 29(1): 108-112.
5 Hutchings D, Hayat A, Karunakaran A, Malik N. Success, safety, and efficacy of the Mynx femoral closure device in a real-world cohort: single-center experience. J Invasive Cardiol. 2016 Mar;28(3):104-108.
6 Noor S, Meyers S, Curl R. Successful reduction of surgeries secondary to arterial access site complications: a retrospective review at a single center with an extravascular closure device. Vasc Endovascular Surg. 2010 Jul;44(5):345-349.
7 Fargen KM, Hoh BL, Mocco J. A prospective randomized single-blind trial of patient comfort following vessel closure: extravascular synthetic sealant closure provides less pain than a self-tightening suture vascular compression device. J NeuroInterv Surg. 2011 Sep; 3(3): 219-223.
† Confirm vessel size is ≥ 5 mm
‡Time to discharge eligibility as compared to manual compression. MATRIX Clinical Trial (IDE# G030182)
IFU
Please refer to the Instructions for Use for complete information, including indications, precautions, warnings, and potential adverse events.
Customer Service and Ordering Information
In the United States, email us your question or order, or call us at 800.327.7714.