Closure devices
Mynxgrip
A wound covering typically made of cross-linked polymer gels in sheet form or an amorphous hydrating gel of various formulations intended to promote wound healing by maintaining a moist wound environment; it may also facilitate wound debridement and/or absorb exudates in wounds that are minimally to moderately exudative. It may combine hydrogel with supplemental dressing materials (e.g., alginate, film backing), require the use of a secondary dressing, and/or provide a barrier impermeable to liquids and gases; it does not include an antimicrobial agent(s). This is a single-use device.
FDA clearances
- PMA P040044 April 2014
Procedures that use closure devices
Frequently asked questions
What is Mynxgrip used for?
A wound covering typically made of cross-linked polymer gels in sheet form or an amorphous hydrating gel of various formulations intended to promote wound healing by maintaining a moist wound environment; it may also facilitate wound debridement and/or absorb exudates in wounds that are minimally to moderately exudative. It may combine hydrogel with supplemental dressing materials (e.g., alginate, film backing), require the use of a secondary dressing, and/or provide a barrier impermeable to liquids and gases; it does not include an antimicrobial agent(s). This is a single-use device.
Who makes Mynxgrip?
Mynxgrip is made by Cordis US Corp.. It is listed under vascular closure devices in our device library.
What sizes does Mynxgrip come in?
The FDA device database does not list sizes for Mynxgrip. Check the instructions for use or ask a Cordis US Corp. representative.
Is Mynxgrip MRI safe?
The FDA device database lists Mynxgrip as MR Safe. Always follow the specific MRI conditions in the labeling.
Is Mynxgrip FDA cleared?
Mynxgrip is covered by FDA submission P040044.
How do I contact a Cordis US Corp. sales representative?
Cordis US Corp. has not listed representatives on LA Vascular yet. Visit the Cordis US Corp. company page for contact details.
Models, sizes and MRI status come from the FDA Global Unique Device Identification Database (GUDID); descriptions marked "provided by the manufacturer" are reviewed before publishing. Not an endorsement; follow the manufacturer's instructions for use.