Guidewires
Forté
by Lake Region Medical Limited
A long, thin, sterile wire intended to be percutaneously placed into the cardiac vasculature (ventricles or coronary vessels) to function as a guide for the introduction, positioning, and/or operation of a device (e.g., catheter, pacing lead); it may also be used in the peripheral vasculature. It may be made of metal (e.g., stainless steel, Nitinol), or polymer and/or glass materials to provide MRI-compatibility, with or without coating, and is available in a variety of distal tip designs. It is used for various diagnostic and interventional procedures, and may include devices used to facilitate manipulation (e.g., torque device). This is a single-use device.
Forté 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 |
|---|---|---|---|
| H7493494901J0 | Outer Diameter .014 in; Length 185 cm | Not stated | Available |
| H7493494902J0 | Outer Diameter .014 in; Length 300 cm | Not stated | Available |
| H7493494903J0 | Outer Diameter .014 in; Length 185 cm | Not stated | Available |
| H7493494904J0 | Outer Diameter .014 in; Length 300 cm | Not stated | Available |
| H7493494905J0 | Outer Diameter .014 in; Length 185 cm | Not stated | Available |
| H7493494906J0 | Outer Diameter .014 in; Length 300 cm | Not stated | Available |
| H7493494907J0 | Outer Diameter .014 in; Length 185 cm | Not stated | Available |
| H7493494908J0 | Outer Diameter .014 in; Length 300 cm | Not stated | Available |
| H7493494909J0 | Outer Diameter .014 in; Length 185 cm | Not stated | Available |
| H7493494910J0 | Outer Diameter .014 in; Length 300 cm | Not stated | Available |
| H74934949010 | Outer Diameter .014 in; Length 185 cm | Not stated | Available |
| H74934949020 | Outer Diameter .014 in; Length 300 cm | Not stated | Available |
| H74934949030 | Outer Diameter .014 in; Length 185 cm | Not stated | Available |
| H74934949040 | Outer Diameter .014 in; Length 300 cm | Not stated | Available |
| H74934949050 | Outer Diameter .014 in; Length 185 cm | Not stated | Available |
| H74934949060 | Outer Diameter .014 in; Length 300 cm | Not stated | Available |
| H74934949070 | Outer Diameter .014 in; Length 185 cm | Not stated | Available |
| H74934949080 | Outer Diameter .014 in; Length 300 cm | Not stated | Available |
| H74934949090 | Outer Diameter .014 in; Length 185 cm | Not stated | Available |
| H74934949100 | Outer Diameter .014 in; Length 300 cm | Not stated | Available |
FDA clearances
- 510(k) K011968 July 2001
Procedures that use guidewires
Frequently asked questions
What is Forté used for?
A long, thin, sterile wire intended to be percutaneously placed into the cardiac vasculature (ventricles or coronary vessels) to function as a guide for the introduction, positioning, and/or operation of a device (e.g., catheter, pacing lead); it may also be used in the peripheral vasculature. It may be made of metal (e.g., stainless steel, Nitinol), or polymer and/or glass materials to provide MRI-compatibility, with or without coating, and is available in a variety of distal tip designs. It is used for various diagnostic and interventional procedures, and may include devices used to facilitate manipulation (e.g., torque device). This is a single-use device.
Who makes Forté?
Forté is made by Lake Region Medical Limited. It is listed under guidewires in our device library.
What sizes does Forté come in?
Sizes listed for Forté: Outer Diameter: 0.01 in; Length: 185–300 cm. Confirm availability with the manufacturer's instructions for use.
Is Forté MRI safe?
The FDA device database entry for Forté does not state its MRI safety status. Check the labeling before MRI.
Is Forté FDA cleared?
Forté is covered by FDA submission K011968.
How do I contact a Lake Region Medical Limited sales representative?
Lake Region Medical Limited has not listed representatives on LA Vascular yet. Visit the Lake Region Medical Limited 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.