Identity
- Trade Name
- Elos Accurate® Hybrid Base™ Engaging FDA UDI
- Generic Name
- Dental implant suprastructure, permanent, preformed FDA UDI
- Device Name
- The Elos Accurate Hybrid Base is a titanium base designed to interface with a dental implant and to support a patient-specific ceramic superstructure or a multi-unit direct restoration cemented to the base. The base and the superstructure form a patient-specific abutment that will support a definitive restoration, either a single crown or a multi-unit restoration. The Elos Accurate Hybrid Base Engaging is intended for single-unit restorations and Elos Accurate Hybrid Base Non-Engaging is intended for multi-unit restorations. Alternatively, a definitive multi-unit restoration may be cemented directly to the Elos Accurate Hybrid Base. FDA UDI
- Model / Reference
- HBE-NBA43-1 FDA UDI
- Description
- The Elos Accurate Hybrid Base is a titanium base designed to interface with a dental implant and to support a patient-specific ceramic superstructure or a multi-unit direct restoration cemented to the base. The base and the superstructure form a patient-specific abutment that will support a definitive restoration, either a single crown or a multi-unit restoration. The Elos Accurate Hybrid Base Engaging is intended for single-unit restorations and Elos Accurate Hybrid Base Non-Engaging is intended for multi-unit restorations. Alternatively, a definitive multi-unit restoration may be cemented directly to the Elos Accurate Hybrid Base. FDA UDI
Identifiers
- Primary DI / UDI-DI
- 05712821000361 FDA UDI
- 510(k) Number
- K191919 FDA UDI
- FDA Product Code
- NHA FDA UDI
- GMDN Term
- Dental implant suprastructure, permanent, preformed FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 872.3630 FDA UDI
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
No
FDA UDI
Single Use
Yes
FDA UDI
Implantable
Yes
FDA UDI
Contains Latex
No
FDA UDI
Prescription Use
Yes
FDA UDI
Over-the-Counter
No
FDA UDI
Convenience Kit
No
FDA UDI
Combination Product
No
FDA UDI
HCT/P
No
FDA UDI
Premarket Exempt
No
FDA UDI
Lot / Batch Number
Yes
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
Yes
FDA UDI
Moist Heat or Steam Sterilization FDA UDI
Category: Dental implant suprastructure, permanent, preformed
Elos Accurate® Hybrid Base™ Engaging by Elos Medtech Pinol A/S — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Dental implant suprastructure, permanent, preformed.
- SPARE CAST. SLEEVE FOR — SWEDEN & MARTINA INC · Class II
- HS/HG Prosthetic System — OSSTEM IMPLANT Co., Ltd. · Class II
- DESS dental smart solutions — TERRATS MEDICAL SL. · Class II
- Diamodent — Diamodent · Class II
- Cemented Abutment — POINTIMPLANT Co., Ltd. · Class II
- GS System — OSSTEM IMPLANT Co., Ltd. · Class II
- Temporary Abutment — Cybermed Inc. · Class II
- EZ Post — Megagen Implant Co. Ltd · Class II
Cleared under the same submission
K191919 also covers:
- Elos Accurate® Hexalobular Prosthetic Screw — Elos Medtech Pinol A/S
- Elos Accurate® Hexalobular Prosthetic Screw — Elos Medtech Pinol A/S
- Elos Accurate® Hexalobular Prosthetic Screw — Elos Medtech Pinol A/S
- Elos Accurate® Hexalobular Prosthetic Screw — Elos Medtech Pinol A/S
- Elos Accurate® Hexalobular Prosthetic Screw — Elos Medtech Pinol A/S
- Elos Accurate® Hexalobular Prosthetic Screw — Elos Medtech Pinol A/S
- Elos Accurate® Hexalobular Prosthetic Screw — Elos Medtech Pinol A/S
- Elos Accurate® Hexalobular Prosthetic Screw — Elos Medtech Pinol A/S
- Elos Accurate® Hexalobular Prosthetic Screw — Elos Medtech Pinol A/S
- Elos Accurate® Hexalobular Prosthetic Screw — Elos Medtech Pinol A/S
- Elos Accurate® Hexalobular Prosthetic Screw — Elos Medtech Pinol A/S
- Elos Accurate® Hexalobular Prosthetic Screw — Elos Medtech Pinol A/S
Authorization Coverage (1 country)
Regulatory Authorizations
United States Pending data
FDA UDI
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class II | Pending data |
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Manufacturer
- Manufacturer
- Elos Medtech Pinol A/S
Sources (1)
- FDA UDI ac2e03d3-e5f8-42e0-8f4e-44f7f4512419 34 fields · synced May 31, 2026