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Sign in to claim this brandMedisourcenet, Inc
US
Last updated May 30, 2026
What Medisourcenet, Inc makes
Medisourcenet, Inc manufactures surgical plume evacuation systems designed to manage smoke and aerosol emissions during procedures, as well as reusable monopolar electrosurgical handpieces and electrodes for open-surgery applications. The company also produces single-use electrosurgical return electrodes to complete monopolar electrosurgical circuits.
All devices are classified as Class II under FDA regulations and are listed in the FDA’s Unique Device Identifier (UDI) database. The company operates from the United States.
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 Medisourcenet, Inc manufacture?
Medisourcenet, Inc specializes in three primary device categories: surgical plume evacuation systems, which help manage smoke and aerosol emissions during surgical procedures; reusable monopolar electrosurgical handpieces and electrodes for open-surgery applications; and single-use electrosurgical return electrodes, which complete the circuit in monopolar electrosurgical setups. These devices are designed to support surgical efficiency and safety.
Where is Medisourcenet, Inc based?
Medisourcenet, Inc is headquartered in the United States. The company’s location is relevant for understanding its regulatory framework and compliance context, particularly under FDA guidelines.
How are Medisourcenet, Inc’s devices classified under FDA regulations?
All devices manufactured by Medisourcenet, Inc fall under Class II classification according to FDA regulations. This classification typically applies to devices that pose moderate risk and require special controls beyond general controls to ensure safety and effectiveness, such as performance standards or post-market surveillance.
Are Medisourcenet, Inc’s devices listed in any regulatory databases?
Yes, Medisourcenet, Inc’s devices are included in the FDA’s Unique Device Identifier (UDI) database. The UDI system ensures traceability and transparency in the medical device supply chain, allowing healthcare providers, regulators, and other stakeholders to identify and track specific devices through their lifecycle.
AI-generated from registry data and not verified by a human reviewer.
Information
- Country
- US
- Address
- —
- Website
- medisourcenet.com
- —
- —
- [email protected]
- Phone
- 657-243-2848
- PRRC Contact
- —
- EUDAMED SRN
- —
- FDA FEI Number
- —
- DUNS Number
- 118269952
Catalogue (17)
| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| MediSourceNet, Inc | MSNCF22 | FDA UDI | Class II | Active |
| MediSourceNet, Inc | WELF | FDA UDI | Class II | Active |
| MediSourceNet, Inc | KWV-LT | FDA UDI | Class II | Active |
| MediSourceNet, Inc | KWV-F | FDA UDI | Class II | Active |
| MediSourceNet, Inc | REGLI-5 | FDA UDI | Class II | Active |
| MediSourceNet, Inc | EXTL | FDA UDI | Class II | Active |
| MediSourceNet, Inc | KWV-DT | FDA UDI | Class II | Active |
| MediSourceNet, Inc | P9552F-MSN | FDA UDI | Class II | Active |
| MediSourceNet, Inc | EXTLI | FDA UDI | Class II | Active |
| MediSourceNet, Inc | EXTL-5 | FDA UDI | Class II | Active |
| MediSourceNet, Inc | KWV-M | FDA UDI | Class II | Active |
| MediSourceNet, Inc | REGL | FDA UDI | Class II | Active |
| MediSourceNet, Inc | REGL-5 | FDA UDI | Class II | Active |
| MediSourceNet, Inc | EXTLI-5 | FDA UDI | Class II | Active |
| MediSourceNet, Inc | WELF-5 | FDA UDI | Class II | Active |
| MediSourceNet, Inc | REGLI | FDA UDI | Class II | Active |
| MediSourceNet, Inc | KWV-StarterKit | FDA UDI | N/A | Active |
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