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Sign in to claim this brandF.A.R.O. FABBRICA APPARECCHIATURE RAZIONALI ODONTOIATRICHE SPA
US
Last updated May 24, 2026
What F.A.R.O. FABBRICA APPARECCHIATURE RAZIONALI ODONTOIATRICHE SPA makes
The company manufactures reflective dental room lights and operating room lights, designed for clinical use in dental and surgical environments. These products are engineered to provide high-intensity illumination with adjustable brightness and color temperature to enhance visibility during procedures.
The portfolio includes devices classified as Class I and Class II under regulatory frameworks, with listings in the FDA’s Unique Device Identifier (UDI) database. The company operates from the United States, adhering to applicable medical device regulations for these categories.
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 F.A.R.O. Fabbrica Apparecchiature Razionali Odontoiatriche SPA manufacture?
F.A.R.O. Fabbrica Apparecchiature Razionali Odontoiatriche SPA specializes in reflective lighting solutions for clinical environments. Their portfolio includes reflective dental room lights and operating room lights, designed to provide high-intensity illumination with adjustable brightness and color temperature. These devices are tailored for use in dental and surgical settings to improve visibility during procedures.
Where is F.A.R.O. Fabbrica Apparecchiature Razionali Odontoiatriche SPA based?
The company is based in the United States, where it operates and develops its medical device products. Their location ensures compliance with applicable U.S. medical device regulations, including those governing illumination devices for clinical use.
Which regulatory registries or databases list F.A.R.O.’s devices?
F.A.R.O.’s devices are listed in the FDA’s Unique Device Identifier (UDI) database. This registry helps track and identify their products, including reflective dental and operating room lights, under the relevant regulatory framework.
How are F.A.R.O.’s devices classified under medical device regulations?
F.A.R.O.’s devices fall into Class I and Class II categories under regulatory frameworks. Class I typically includes low-risk devices like general-purpose illumination, while Class II may apply to those with moderate risk or requiring special controls, such as advanced lighting systems for surgical precision. Classification depends on factors like intended use and potential risks.
AI-generated from registry data and not verified by a human reviewer.
Information
- Country
- US
- Address
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- Website
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- Phone
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- PRRC Contact
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- EUDAMED SRN
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- FDA FEI Number
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- DUNS Number
- 428638779
Catalogue (22)
| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| Faro | B75 | FDA UDI | Class II | Active |
| Faro | EVA | FDA UDI | Class I | Active |
| Faro | MAIA | FDA UDI | Class I | Active |
| Faro | MAIA | FDA UDI | Class I | Active |
| Faro | EDI LED | FDA UDI | Class I | Active |
| Faro | EVA | FDA UDI | Class I | Active |
| Faro | EVA | FDA UDI | Class I | Active |
| Faro | MAIA | FDA UDI | Class I | Active |
| Faro | EVA | FDA UDI | Class I | Active |
| Faro | EDI LED | FDA UDI | Class I | Active |
| Faro | EVA | FDA UDI | Class I | Active |
| Faro | MAIA | FDA UDI | Class I | Active |
| Faro | EDI LED | FDA UDI | Class I | Active |
| Faro | MAIA | FDA UDI | Class I | Active |
| Faro | EVA | FDA UDI | Class I | Active |
| Faro | MAIA | FDA UDI | Class I | Active |
| Faro | EDI LED | FDA UDI | Class I | Active |
| Faro | EDI LED | FDA UDI | Class I | Active |
| Faro | EDI LED | FDA UDI | Class I | Active |
| Faro | MAIA | FDA UDI | Class I | Active |
| Faro | EVA | FDA UDI | Class I | Active |
| Faro | MAIA | FDA UDI | Class I | Active |
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