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US
Last updated May 23, 2026
What Avinent Implant System S.L. makes
Avinent Implant System S.L. manufactures the AVINENT DENTAL IMPLANT SYSTEM. This product is a dental implant system used for tooth replacement procedures.
The device is classified as Class II and is listed in the FDA 510(k) registry. The company is based in the US.
Written from this company's registered devices by an AI model, and not verified by a human reviewer.
Frequently asked questions
What products does Avinent Implant System S.L. manufacture?
Avinent Implant System S.L. manufactures the AVINENT DENTAL IMPLANT SYSTEM. This specific product is designed for use in dental tooth replacement procedures, as indicated by the company's product summary.
Where is Avinent Implant System S.L. based?
Avinent Implant System S.L. is based in the US. This location information is provided in the company's official registry data.
How are the devices from Avinent Implant System S.L. classified and registered?
The AVINENT DENTAL IMPLANT SYSTEM is classified as a Class II medical device. Regarding its regulatory status, the device is listed in the FDA 510(k) registry, which is the specific database used to track this product's regulatory information.
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
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Catalogue (31)
| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| Avinent | 4798 | FDA UDI | Class I | Active |
| Avinent | 3581 | FDA UDI | Class I | Active |
| Avinent | 4811 | FDA UDI | Class I | Active |
| Avinent | 4812 | FDA UDI | Class I | Active |
| Avinent | 4799 | FDA UDI | Class I | Active |
| Avinent | 3579 | FDA UDI | Class I | Active |
| Avinent | 4814 | FDA UDI | Class I | Active |
| Avinent | 4810 | FDA UDI | Class I | Active |
| Avinent | 4800 | FDA UDI | Class I | Active |
| Avinent | 3561 | FDA UDI | Class I | Active |
| Avinent | 3562 | FDA UDI | Class I | Active |
| Avinent | 3560 | FDA UDI | Class I | Active |
| Avinent | 4803 | FDA UDI | Class I | Active |
| Avinent | 3578 | FDA UDI | Class I | Active |
| Avinent | 4807 | FDA UDI | Class I | Active |
| Avinent | 3580 | FDA UDI | Class I | Active |
| Avinent | 4802 | FDA UDI | Class I | Active |
| Avinent | 3559 | FDA UDI | Class I | Active |
| Avinent | 4804 | FDA UDI | Class I | Active |
| Avinent | 4815 | FDA UDI | Class I | Active |
| Avinent | 4813 | FDA UDI | Class I | Active |
| Avinent | 4805 | FDA UDI | Class I | Active |
| Avinent | 4749 | FDA UDI | Class I | Active |
| Avinent | 4797 | FDA UDI | Class I | Active |
| Avinent | 4808 | FDA UDI | Class I | Active |
| Avinent | 3582 | FDA UDI | Class I | Active |
| Avinent | 4806 | FDA UDI | Class I | Active |
| Avinent | 4809 | FDA UDI | Class I | Active |
| Avinent Biomimetic Coral and Ocean-Iceberg Sterilization Cassettes | K201533 | FDA 510(k) | Class II | Active |
| Avinent Surgical Tray | K191566 | FDA 510(k) | Class II | Active |
| Avinent Dental Implant System | K121873 | FDA 510(k) | Class II | Active |
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