Search Results

NobelActive® S TiUltra™, NobelActive® S TiUnite®

NobelActive® S TiUltra™ and NobelActive® S TiUnite® implants are endosseous implants intended to be surgically placed in the upper or lower jaw bone for anchoring or supporting tooth replacements to restore patient esthetics and chewing function.

NobelActive® S TiUltra™ and NobelActive® S TiUnite® implants are indicated for single or multiple unit restorations in splinted or non-splinted applications.

This can be achieved by a 2-stage or 1-stage surgical technique in combination with immediate, early or delayed loading protocols, recognizing sufficient primary stability and appropriate occlusal loading for the selected technique.

NobelReplace® S TiUltra™, NobelReplace® S TiUnite®

NobelReplace® S TiUltra™ and NobelReplace® S TiUnite® implants are endosseous dental implants intended to be surgically placed in the bone of the upper or lower jaw arches to provide support for prosthetic devices, such as an artificial tooth, in order to restore patient esthetics and chewing function.

The NobelReplace® S TiUltra™ and NobelReplace® S TiUnite® implants are indicated for single or multiple unit restorations.

The NobelReplace® S TiUltra™ and NobelReplace® S TiUnite® implants can be used in splinted or non-splinted applications.

The NobelReplace® S TiUltra™ and NobelReplace® S TiUnite® implants may be placed immediately and put into immediate function provided that initial stability requirements detailed in the manual are satisfied.

NobelParallel™ S TiUltra™, NobelParallel™ S TiUnite®

NobelParallel™ S TiUltra™ and NobelParallel™ S TiUnite® implants are endosseous implants intended to be surgically placed in the upper or lower jaw bone for anchoring or supporting replacements to restore patient esthetics and chewing function.

NobelParallel™ S TiUltra™ and NobelParallel™ S TiUnite® implants are indicated for single or multiple restorations in splinted or non-splinted applications.

This can be achieved by 2-stage or 1-stage surgical techniques in combination with immediate, early or delayed loading protocols, recognizing sufficient primary stability and appropriate occlusal loading for the selected technique.

Implants with <7 mm length are for delayed loading only when appropriate stability has been achieved.

The Subject Device, Nobel Biocare S Series Implants, comprises of six Device Lines NobelActive S TiUltra™, NobelParallel™ S TiUltra™, NobelReplace S TiUltra™, NobelActive S TiUnite, NobelParallel™ S TiUnite, NobelReplace S TiUnite.

Nobel Biocare S Series Implants are intended for use as an endosseous dental implant in the maxilla or mandible for anchoring or supporting dental prostheses to restore chewing function. The Subject Device features a consistent diameter at the implant-abutment interface, regardless of the implant size or type. This means that the prosthetic components, such as abutments and restorative elements, have uniform dimensions and connections across all implant sizes within the system. The connection used is the Narrow Platform (NP) conical connection.

The implant bodies of the Subject Devices and Predicate devices are the same. This allows use of the same drills and drilling protocols, rescue procedures and rescue tools. By using the existing Narrow Platform connection, the same prosthetic workflows, prosthetic components, and lab components can be used.

The implants are available in different sizes as listed in Table 1.

The Nobel Biocare S Series Implants are manufactured from commercially pure titanium and incorporate a conical connection (Size Narrow Platform (NP)) with a hex interface in the collar region, which combines with Nobel Biocare's existing prosthetic Abutment portfolio cleared in K071370, K083100, K132746, K233208, K202344, K200040, K132749, K161416, K202452, K240346, K041236, K133731, K061003 and K161435.

Table 2 outlines which single-unit restoration abutments with an NP connection can be used with the subject device.

Table 3 outlines which multi-unit restoration abutments and bridges with an NP connection can be used with the subject devices.

Table 4 outlines the temporary and healing restorations with an NP connection that can be used with the subject devices.

Table 5 lists the corresponding submissions where compatible Class II accessories with an NP connection were previously identified.

The On1™ Base/On1™ Base Xeal must not be used in combination with NobelActive® S, NobelParallel™ S, NobelReplace® S implants.

NobelActive® S, NobelParallel™ S, NobelReplace® S implants in combination with NobelProcera® Angulated Screw Channel Abutment and NobelProcera® FCZ Implant Crown are indicated for maxillary lateral and mandibular central/lateral incisors only.

NobelActive® S, NobelParallel™ S, NobelReplace® S implants may be used in combination with NobelProcera® Angulated Screw Channel Abutment and NobelProcera® FCZ Implant Crown up to a maximum angulation of 20°

NobelActive® S, NobelParallel™ S, NobelReplace® S implants may be used in combination with GoldAdapt Engaging CC NP abutments in straight (0°) configurations only.

No angulation is allowed for Universal Base Conical Connection Abutments when mated with the NobelActive® S, NobelParallel™ S, NobelReplace® S implants with diameters greater than 3.5mm.

N/A

Ask a specific question about this device

The TiGEN Abutment, PMMA Abutment and Scan Healing Abutment are intended for use on endosseous dental implants in the edentulous or partially edentulous maxilla or mandible, as an aid in prosthetic rehabilitation.

The PMMA Abutment is indicated to be used pror to the final components to maintain, stabilize and shape the soft tissue during the healing plase. They must be placed out of occlusion and are for temporary use (3 months).

For TiGEN Abutment and PMMA Abutment, all digitally designed abutments for use with PMMA Abutment and TiGEN Abutment are intended to be sent to a MegaGen-validated milling center for manufacture.

The TiGEN Abutment is machined with the final prosthetic in accordance with the intraoral structure. It is machined by using dental CAD/CAM technology in accordance with customized patient's information in MegaGen-validated milling center. The TiGEN Abutment is made of Ti-6Al-4V ELI alloy. And It is provided with abutment screw. All TiGEN Abutment is provided non-sterile. The milled TiGEN Abutment must be sterilized by users prior to use.

The PMMA Abutment is a temporary prosthesis used until the final prosthesis is placed for up to three months. The PMMA Post is machined with the temporary prosthetic in accordance with the intraoral structure by using dental CAD/CAM technology. The PMMA Cuff is made of Ti-6Al-4V ELI alloy and available in various gingival heights. The PMMA Post is made of Polymethyl methacrylate and available in various diameters and lengths so that it can be used according to individual patient conditions. All PMMA Abutment is provided non-sterile with abutment screw. The milled PMMA Abutment must be sterilized by users prior to use.

The Scan Healing Abutment designed to aid in soft tissue contouring during the healing period after implant placement, creating an emergence profile for the final prosthesis. And they have the added design feature to be scannable an intraoral impression by digital scanner. The Scan Healing Abutment is provided with abutment screw and is provided gamma-sterile.

This document pertains to a 510(k) premarket notification for dental implant abutments and does not contain information about an AI/ML medical device. Therefore, a table of acceptance criteria and a study proving the device meets the criteria, as requested by the prompt, cannot be extracted from the provided text for an AI/ML context.

The document discusses the substantial equivalence of the "TiGEN Abutment, PMMA Abutment and Scan Healing Abutment" to already marketed predicate devices. The studies mentioned are primarily bench tests, biocompatibility evaluations, and sterilization/shelf-life validations, which are standard for physical medical devices. There is no mention of an AI/ML component, AI/ML device performance metrics, or related study methodologies like multi-reader multi-case (MRMC) studies.

Without information on an AI/ML component, the requested details such as sample size for test sets (for AI), data provenance, expert ground truth establishment, MRMC studies, standalone AI performance, and training set details are not applicable and cannot be provided.

Ask a specific question about this device

ICX-Implant System is indicated for use in partially or fully edentulous patients to support maxillary and mandibular single-unit, multiple-unit, and overdenture dental restorations. ICX- Implant System is indicated for immediate loading when good primary stability is achieved and with appropriate occlusal loading. Implants with lengths less than 7.0 mm are indicated for delayed loading only.

ICX-Implant System CAD CAM abutments are intended for use with dental implants as a support for single unit or multiple unit prostheses in the maxilla of a partially or fully edentulous patient. All digitally designed abutments for use with ICX-Implant System CAD CAM abutments are intended to be manufactured at a medentis medical GmbH validated milling center.

The purpose of this submission is to obtain marketing clearance for an endosseous dental implant and abutment system. ICX-Implant System, from medentis medical GmbH. The ICX-Implant System includes a range of endosseous dental implants and prosthetic components. All implants have a selftapping apical thread with a tapered body and root-form designs with an internal hex implant/abutment connection. The implant body surface is blasted and acid-etched.

Abutments are available in multiple designs, including straight and angled abutments intended for single tooth and multi-unit restorations.

The provided text is a 510(k) summary for the "ICX-Implant System." This document is a premarket notification for a medical device and, as such, focuses on demonstrating substantial equivalence to previously cleared devices rather than proving the device meets specific acceptance criteria through a standalone performance study.

Therefore, the document does not contain the detailed information required to fully answer all aspects of your request, especially regarding specific acceptance criteria for AI/algorithm performance, multi-reader multi-case studies, or detailed ground truth establishment for a test/training set in the context of an AI device.

The document does describe non-clinical performance data for the dental implant system itself (e.g., sterilization, biocompatibility, mechanical testing) to show its safety and effectiveness, but not for an AI component.

Here's an analysis based on the provided text, highlighting what is present and what is missing:

1. A table of acceptance criteria and the reported device performance:

• Missing: The document does not define "acceptance criteria" in the context of an AI/algorithm's performance (e.g., sensitivity, specificity, AUC). Instead, it discusses the substantial equivalence of the ICX-Implant System and its components to predicate devices based on technological characteristics, materials, and indications for use.

• The "Performance Data" section (Page 7) lists non-clinical tests performed, such as:

  • Validation of gamma irradiation sterilization to a sterility assurance level (SAL) of 10⁻⁶.
  • Bacterial endotoxin testing: < 20 EU/device.
  • Validation of moist heat sterilization cycle to SAL of 10⁻⁶.
  • Shelf life testing confirming seal integrity and sterility after 5 years.
  • Biocompatibility testing (in vitro cytotoxicity).
  • Characterization of implant surface (SEM, surface chemistry, hydrophilicity).
  • Mechanical testing according to ISO 14801 (static and dynamic loading).
  • Analysis of surface area and initial bone to implant contact area.
  • MR compatibility testing (supporting MR Conditional labeling).

  These are performance requirements for a dental implant and are confirmed to have been met, but they are not "acceptance criteria" for an AI algorithm's diagnostic performance.

2. Sample size used for the test set and the data provenance (e.g., country of origin of the data, retrospective or prospective):

• Missing: No information on test set size or data provenance for an AI/algorithm is provided. The document explicitly states: "No clinical data were included in this submission" (Page 8). The non-clinical tests listed above would have had specific sample sizes for those tests (e.g., number of implants for mechanical testing), but these are not detailed in the summary beyond stating the tests were performed "accordance with" relevant standards.

3. Number of experts used to establish the ground truth for the test set and the qualifications of those experts:

• Missing: Not applicable as no AI/algorithm performance test set is described.

4. Adjudication method (e.g., 2+1, 3+1, none) for the test set:

• Missing: Not applicable as no AI/algorithm performance test set is described.

5. If a multi-reader multi-case (MRMC) comparative effectiveness study was done, If so, what was the effect size of how much human readers improve with AI vs without AI assistance:

• Missing: No MRMC study was done, as no AI component is mentioned.

6. If a standalone (i.e. algorithm only without human-in-the-loop performance) was done:

• Missing: No standalone algorithm performance study was done, as no AI component is mentioned.

7. The type of ground truth used (expert consensus, pathology, outcomes data, etc.):

• Missing: Not applicable as no AI/algorithm performance is described. The "ground truth" for the implant itself is its conformance to material standards, mechanical properties, and biocompatibility, as verified by laboratory tests.

8. The sample size for the training set:

• Missing: No training set for an AI/algorithm is mentioned.

9. How the ground truth for the training set was established:

• Missing: No training set for an AI/algorithm is mentioned.

In summary:

This 510(k) pertains to a dental implant system (a physical device) and its components (e.g., abutments), not a software as a medical device (SaMD) or an AI-powered diagnostic/assistance tool. The entire submission is built on demonstrating substantial equivalence to existing, legally marketed predicate devices through a comparison of their technological characteristics, materials, and non-clinical performance data relevant to the physical implant and its function. It explicitly states that "No clinical data were included in this submission," further confirming that no human-in-the-loop or standalone diagnostic performance studies (which would be typical for AI/ML devices) were conducted or are required for this type of submission.

Ask a specific question about this device