Ablation systems
Solero
A component of a microwave hyperthermia system designed to be placed inside the body to deliver microwave energy to produce a systemic or local heating effect. It is also referred to as an interstitial applicator or probe and is typically a catheter-enclosed conductor of microwave energy that is introduced into the body either manually or endoscopically. It typically includes a thermometry component that monitors the temperature of the device during operation. This is a single-use device.
Solero 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 |
|---|---|---|---|
| 12740000US | — | MR Unsafe | Available |
| 700106001-US | Length 14 cm | MR Unsafe | Available |
| 700106002-US | Length 19 cm | MR Unsafe | Available |
| 700106003-US | Length 29 cm | MR Unsafe | Available |
| H787127401380 | — | Not stated | Available |
FDA clearances
- 510(k) K182250 February 2019
- 510(k) K162449 May 2017
Procedures that use ablation systems
Frequently asked questions
What is Solero used for?
A component of a microwave hyperthermia system designed to be placed inside the body to deliver microwave energy to produce a systemic or local heating effect. It is also referred to as an interstitial applicator or probe and is typically a catheter-enclosed conductor of microwave energy that is introduced into the body either manually or endoscopically. It typically includes a thermometry component that monitors the temperature of the device during operation. This is a single-use device.
Who makes Solero?
Solero is made by AngioDynamics, Inc.. It is listed under tumor ablation systems (microwave, rf, cryo) in our device library.
What sizes does Solero come in?
Sizes listed for Solero: Length: 14–29 cm. Confirm availability with the manufacturer's instructions for use.
Is Solero MRI safe?
The FDA device database lists Solero as MR Unsafe. Always follow the specific MRI conditions in the labeling.
Is Solero FDA cleared?
Solero is covered by FDA submissions K162449, K182250.
How do I contact a AngioDynamics, Inc. sales representative?
AngioDynamics, Inc. has not listed representatives on LA Vascular yet. Visit the AngioDynamics, Inc. 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.