Closure devices
Manta
An implantable, bioabsorbable device designed for haemostasis/closure of a puncture site, through pressure/compression, on a patient having undergone femoral artery catheterization; it is intended as an alternative to manual compression or surgical techniques to reduce the time to haemostasis. It consists of an animal-derived collagen plug that is implanted using an included delivery device (e.g., guidewire, hand-held delivery unit) onto the extravascular surface of the femoral artery access site (top of arteriotomy site), and may be held in place with an included synthetic, bioabsorbable patch/anchor/suture to achieve haemostasis.
Manta models and sizes
From the FDA Global Unique Device Identification Database. Confirm with the manufacturer's instructions for use.
| Model / catalog no. | Size | MRI | Status |
|---|---|---|---|
| IPN923491 | — | MR Conditional | Available |
| IPN923493 | — | MR Conditional | Available |
| IPN923494 | — | MR Conditional | Available |
| IPN923496 | — | MR Conditional | Available |
| IPN930507 | — | MR Conditional | Available |
| IPN930509 | — | MR Conditional | Available |
| IPN930511 | — | MR Conditional | Available |
| IPN930513 | — | MR Conditional | Available |
FDA clearances
- PMA P180025 May 2020
Procedures that use closure devices
Frequently asked questions
What is Manta used for?
An implantable, bioabsorbable device designed for haemostasis/closure of a puncture site, through pressure/compression, on a patient having undergone femoral artery catheterization; it is intended as an alternative to manual compression or surgical techniques to reduce the time to haemostasis. It consists of an animal-derived collagen plug that is implanted using an included delivery device (e.g., guidewire, hand-held delivery unit) onto the extravascular surface of the femoral artery access site (top of arteriotomy site), and may be held in place with an included synthetic, bioabsorbable patch/anchor/suture to achieve haemostasis.
Who makes Manta?
Manta is made by Teleflex Incorporated. It is listed under vascular closure devices in our device library.
What sizes does Manta come in?
The FDA device database does not list sizes for Manta. Check the instructions for use or ask a Teleflex Incorporated representative.
Is Manta MRI safe?
The FDA device database lists Manta as MR Conditional. Always follow the specific MRI conditions in the labeling.
Is Manta FDA cleared?
Manta is covered by FDA submission P180025.
How do I contact a Teleflex Incorporated sales representative?
Teleflex Incorporated has not listed representatives on LA Vascular yet. Visit the Teleflex Incorporated 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.