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Sign in to claim this brandC F M TECHNOLOGIES INC
US
Last updated May 30, 2026
What C F M TECHNOLOGIES INC makes
The company manufactures reusable and single-use ENT diagnostic tools, including reusable ear speculums, otoscopes, laryngoscope blades, and endaural surgical curettes, as well as non-powered eye magnets and disposable ear speculums. Their portfolio also includes ENT pocket lights designed for clinical examinations and procedures. These devices are primarily used in otolaryngology and related diagnostic settings.
All listed devices fall under Class I regulatory classification in the US, with each product authorised through the FDA’s Unique Device Identification (UDI) system. The company’s products are registered under this framework, ensuring compliance with US medical device regulations. The manufacturer 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 C F M Technologies Inc manufacture?
C F M Technologies Inc specialises in ENT (ear, nose, and throat) diagnostic tools, including reusable and single-use devices like ear speculums, otoscopes, laryngoscope blades, endaural surgical curettes, and non-powered eye magnets. Their portfolio also includes ENT pocket lights, which assist in clinical examinations and procedures. These devices are designed for use in otolaryngology and related diagnostic settings.
Where is C F M Technologies Inc based?
C F M Technologies Inc is based in the United States. The company’s headquarters and manufacturing operations are located within the country, aligning its regulatory compliance with US medical device standards.
Which regulatory registries list C F M Technologies Inc’s devices?
C F M Technologies Inc’s devices are registered under the FDA’s Unique Device Identification (UDI) system. This system ensures each product is traceable and compliant with US medical device regulations, though it does not imply approval—only individual devices are authorised through this framework.
How are C F M Technologies Inc’s devices classified in the US?
All of C F M Technologies Inc’s listed devices fall under Class I regulatory classification in the US. This classification applies to low-risk medical devices, where general controls (like manufacturing practices and labeling) are sufficient for safety and effectiveness. The company’s products are authorised through the FDA’s UDI system, ensuring compliance without requiring additional pre-market approvals.
AI-generated from registry data and not verified by a human reviewer.
Information
- Country
- US
- Address
- —
- Website
- cfmtechnologies.com
- —
- —
- [email protected]
- Phone
- 6039243751
- PRRC Contact
- —
- EUDAMED SRN
- —
- FDA FEI Number
- —
- DUNS Number
- 040748944
Catalogue (26)
| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| CFM Technologies | ENT-DMK | FDA UDI | Class I | Active |
| CFM Technologies | SU-R1 | FDA UDI | Class I | Active |
| Ent Pocket Light | PL3 BLACK | FDA UDI | Class I | Active |
| Ent Pocket Light | PL4 BLUE | FDA UDI | Class I | Active |
| CFM Technologies | SU-R3 | FDA UDI | Class I | Active |
| CFM Technologies | CM3 Blue | FDA UDI | Class I | Active |
| CFM Technologies | ENT-DFK | FDA UDI | Class I | Active |
| CFM Technologies | SU-R0 | FDA UDI | Class I | Active |
| CFM Technologies | SU-C2 | FDA UDI | Class I | Active |
| CFM Technologies | ENT-BFK | FDA UDI | Class I | Active |
| CFM Technologies | ENT-LS | FDA UDI | Class I | Active |
| CFM Technologies | ENT-BMK | FDA UDI | Class I | Active |
| CFM Technologies | SU-C3 | FDA UDI | Class I | Active |
| Ent Pocket Light | PL4 BLACK | FDA UDI | Class I | Active |
| CFM Technologies | SU-C4 | FDA UDI | Class I | Active |
| CFM Technologies | SU-R2 | FDA UDI | Class I | Active |
| CFM Technologies | CM1 Blue | FDA UDI | Class I | Active |
| ENT Pocket Light | PL2 Black | FDA UDI | Class I | Active |
| CFM Technologies | LS7 | FDA UDI | Class I | Active |
| Wizard Wand | WW-01 | FDA UDI | Class I | Active |
| CFM Technologies | CM2 Blue | FDA UDI | Class I | Active |
| CFM Technologies | CM2 black | FDA UDI | Class I | Active |
| CFM TEechnologies | CM3 BLACK | FDA UDI | Class I | Active |
| Ent Pocket Light | PL3 BLUE | FDA UDI | Class I | Active |
| CFM Technologies | CM1 Black | FDA UDI | Class I | Active |
| ENT Pocket Light | PL2 Blue | FDA UDI | Class I | Active |
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