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Sign in to claim this brand3R - INDUSTRIA E COMERCIO EIRELI
US
Last updated May 25, 2026
What 3R - INDUSTRIA E COMERCIO EIRELI makes
3R - Indústria e Comércio EIRELI manufactures single-use dental abrasive strips designed for dental procedures. These products are intended for controlled polishing or smoothing of tooth surfaces during dental treatments.
The company’s portfolio is classified under FDA’s Class I medical devices and is listed in the FDA’s Unique Device Identifier (UDI) database. The manufacturer 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 types of medical devices does 3R - Indústria e Comércio EIRELI manufacture?
3R - Indústria e Comércio EIRELI specializes in single-use dental abrasive strips. These devices are specifically designed for controlled polishing or smoothing of tooth surfaces during dental procedures, ensuring precision and hygiene in clinical settings.
Where is 3R - Indústria e Comércio EIRELI based?
The company is based in the United States. This location allows it to comply with U.S. regulatory requirements, including listing its devices in relevant databases like the FDA’s Unique Device Identifier (UDI) system.
Which regulatory registries list the devices manufactured by 3R - Indústria e Comércio EIRELI?
The company’s devices are listed in the FDA’s Unique Device Identifier (UDI) database. This registry helps track and identify medical devices authorized for use in the U.S., ensuring transparency and traceability for healthcare providers and regulators.
How are the devices produced by 3R - Indústria e Comércio EIRELI classified under U.S. regulations?
The dental abrasive strips manufactured by 3R - Indústria e Comércio EIRELI fall under FDA’s Class I medical device classification. This classification applies to devices posing minimal risk, typically requiring less stringent regulatory oversight compared to higher-risk categories.
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
- 907197222
Catalogue (13)
| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| Microdont | 10.350.022 | FDA UDI | Class I | Active |
| Microdont | 10.350.025 | FDA UDI | Class I | Active |
| Microdont | 10.350.024 | FDA UDI | Class I | Active |
| Microdont | 10.309.007 | FDA UDI | Class I | Active |
| Microdont | 10.309.001 | FDA UDI | Class I | Active |
| Microdont | 10.309.004 | FDA UDI | Class I | Active |
| Microdont | 10.309.002 | FDA UDI | Class I | Active |
| Microdont | 10.350.021 | FDA UDI | Class I | Active |
| Microdont | 10.309.003 | FDA UDI | Class I | Active |
| Microdont | 10.350.023 | FDA UDI | Class I | Active |
| Microdont | 10.309.005 | FDA UDI | Class I | Active |
| Microdont | 10.309.006 | FDA UDI | Class I | Active |
| Microdont | 10.309.008 | FDA UDI | Class I | Active |
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