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Sign in to claim this brandArrinex, Inc.
US
Last updated May 30, 2026
What Arrinex, Inc. makes
Arrinex, Inc. manufactures general cryosurgical systems that use cryogen gas and mechanical components, including nitrous oxide gas cartridges. Their product line includes the ClariFix and ClariFix Device, which are designed for cryosurgical applications.
These devices are classified as Class II medical devices and are listed in the FDA 510(k) and FDA UDI registries. The company is based in 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 does Arrinex, Inc. make?
Arrinex, Inc. manufactures general cryosurgical systems that use cryogen gas and mechanical components, including nitrous oxide gas cartridges. Their product line includes the ClariFix and ClariFix Device, which are designed for cryosurgical applications.
Where is Arrinex, Inc. based?
Arrinex, Inc. is based in the United States, as stated in the company's country of origin within the provided device data.
Which regulatory registries list Arrinex, Inc.'s devices?
Arrinex, Inc.'s devices are listed in the FDA 510(k) and FDA UDI registries, as explicitly noted in the LISTED IN field of the device data.
How are Arrinex, Inc.'s devices classified?
Arrinex, Inc.'s devices are classified as Class II medical devices, according to the DEVICE CLASSES field in the provided data, which specifies this classification for their cryosurgical systems and related components.
AI-generated from registry data and not verified by a human reviewer.
Information
- Country
- US
- Address
- —
- Website
- arrinex.com
- —
- —
- [email protected]
- Phone
- 650-468-6176
- PRRC Contact
- —
- EUDAMED SRN
- —
- FDA FEI Number
- —
- DUNS Number
- 079807364
Catalogue (8)
| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| ClariFix | CFX-1002 | FDA UDI | Class II | Active |
| ClariFix | CFX-0004 | FDA UDI | Class II | Active |
| ClariFix | CFX-1000 | FDA UDI | Class II | Active |
| ClariFix | CFX-0001 | FDA UDI | Class II | Active |
| ClariFix | CFX-0003 | FDA UDI | Class II | Unknown |
| ClariFix | K190356 | FDA 510(k) | Class II | Active |
| ClariFix Device | K162608 | FDA 510(k) | Class II | Active |
| ClariFix Device | K160669 | FDA 510(k) | Class II | Active |
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