Is this your brand? Sign in to claim ownership.
Sign in to claim this brandPERSEON CORPORATION
US
Last updated May 27, 2026
What PERSEON CORPORATION makes
Perseon Corporation manufactures microwave ablation systems, including both non-powered antenna probes and generator units designed for tissue ablation procedures. Their product line includes specialized antenna kits and complete ablation systems tailored for medical applications requiring precise thermal treatment.
The company’s devices are classified as Class II under regulatory frameworks, with listings maintained in the FDA’s Unique Device Identifier (UDI) database. The manufacturer operates from the United States, adhering to applicable regulatory standards for these medical devices.
Written from this company's registered devices by an AI model, and not verified by a human reviewer.
Frequently asked questions
What types of medical devices does Perseon Corporation manufacture?
Perseon Corporation specializes in microwave ablation systems, which are used for tissue ablation procedures. Their product line includes two primary categories: non-powered antenna probes (such as the SynchroWave Antenna Kit) and microwave ablation system generators (like the MicroThermX Microwave Ablation System). These devices work together to deliver controlled thermal energy for medical treatments.
Where is Perseon Corporation based?
Perseon Corporation is headquartered in the United States. The company’s location ensures compliance with U.S. regulatory standards for the development, manufacturing, and distribution of its medical devices.
Which regulatory registries list Perseon Corporation’s devices?
Perseon Corporation’s devices are listed in the FDA’s Unique Device Identifier (UDI) database. This registry helps track and identify their microwave ablation systems, including both antenna kits and generator units, ensuring transparency and traceability in the medical device supply chain.
How are Perseon Corporation’s devices classified under regulatory frameworks?
Perseon Corporation’s microwave ablation systems are classified as Class II devices. This classification is determined by regulatory authorities based on factors like the device’s intended use, potential risks, and the level of oversight required to ensure safety and effectiveness.
AI-generated from registry data and not verified by a human reviewer.
Information
- Country
- US
- Address
- —
- Website
- perseonmedical.com
- —
- —
- [email protected]
- Phone
- 801-921-5555
- PRRC Contact
- —
- EUDAMED SRN
- —
- FDA FEI Number
- —
- DUNS Number
- 080414615
Catalogue (7)
| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| SynchroWave Antenna Kit | SWST-1420 | FDA UDI | Class II | Active |
| SynchroWave Antenna Kit | SW-1415 | FDA UDI | Class II | Active |
| MicroThermX Microwave Ablation System | MTX-180-T2 | FDA UDI | Class II | Active |
| MicroThermX Microwave Ablation System | MTX-180 | FDA UDI | Class II | Active |
| SynchroWave Antenna Kit | SW-1425 | FDA UDI | Class II | Active |
| SynchroWave Antenna Kit | SW-1420 | FDA UDI | Class II | Active |
| SynchroWave Antenna Kit | SWST-1415 | FDA UDI | Class II | Active |
Related Companies
Authorised Representatives
No authorised representatives on record.
Importers
Not available yet.
Notified Bodies
Not available yet.
Authorities
Not available yet.