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MosdentISTANBUL 1992
// Implants

What is a Smart Implant? Technological Transformation in New Generation Dental Treatment

A smart implant is a titanium implant with a hydrophilic surface and digital planning; in five randomised trials the surface showed no clinical advantage.

Dr Ömer Faruk Şarkbay, PhDWritten by
Published
5 minread
Dr Hakan Kavalmedical review
Titanium implant screw standing upright beside two ceramic crowns on a blue surface
Implants·5 min
// Quick answer

A smart implant is a titanium dental implant sold together with a modified surface and a digital workflow rather than a separate implant category: hydrophilic surface chemistry that wets faster with blood and proteins, computer-guided or robot-assisted placement planning, and in a few systems biosensors for follow-up. The claimed benefit is faster osseointegration, yet a systematic review of five randomised trials covering 246 implants found no clinically significant difference in implant stability or survival between a hydrophilic surface and a conventional sandblasted, acid-etched surface (PubMed 32450983).

// Key takeaways
  • 01Smart implant is not a regulatory class: it labels a titanium implant combined with hydrophilic surface treatment, digital or robot-assisted planning and, in some systems, biosensor follow-up.
  • 02Hydrophilic surfaces did not show a clinically significant advantage in implant stability or survival over conventional sandblasted, acid-etched surfaces across 5 randomised trials and 246 implants, with stability measured at baseline and at 3, 6 and 8 weeks (PubMed 32450983).
  • 03Computer-guided placement carries a measured error budget: pooled mean deviation across 67 studies was 1.11 mm at the entry point, 1.40 mm at the apex and 3.51 degrees in angulation, with robot-assisted systems lowest at 0.81 mm, 0.77 mm and 1.71 degrees (PubMed 38509530).
  • 04In a prospective series of 25 hydrophilic bone-level tapered implants placed immediately in posterior sites, 24 of 25 (96 percent) survived a mean of 57 plus or minus 8.07 months; the leading prosthetic complication was proximal contact loss at 41.67 percent (PubMed 38454439).
  • 05The exclusions do not change with the surface: ongoing chemotherapy or radiotherapy, uncontrolled diabetes and advanced osteoporosis remain the contraindications listed for implant placement.

Smart Implant Is a Name for a Combination of Technologies

A smart implant is a titanium dental implant that is sold together with a modified surface and a digital workflow. The implant body is the same metal used in conventional systems, and it still replaces the root of a missing tooth by fusing with the jawbone. What the term adds is a package of features around that body: a hydrophilic, water-attracting surface chemistry, computer-guided or robot-assisted planning of the implant position, and in a small number of systems biosensors intended for follow-up after placement.

There is no regulatory class called smart implant. The label is used by manufacturers and clinics to describe implants that carry one or more of these features, so two products sold under the same name can differ considerably. For a patient this means the useful question is which of the features a given system actually has, and what each feature has been shown to change in measured outcomes.

The features are worth separating because the evidence behind them is uneven. Digital planning has a large body of measured accuracy data. The hydrophilic surface has been tested in randomised trials against a conventional surface, with results that are more modest than the marketing suggests. Biosensor follow-up is at an early stage and has little published clinical data, so in daily practice the implant is still followed with clinical examination and X-rays. The treatment steps, the suitability criteria and the healing process are otherwise the same as for any implant.

What the Hydrophilic Surface Is Designed to Do

Most conventional implants have a sandblasted, acid-etched titanium surface. That treatment roughens the metal so bone cells can attach, but the surface itself tends to repel water. A hydrophilic surface is processed so that it wets quickly: when the implant is placed, blood and proteins spread across it faster. The design idea is that faster early contact with blood and healing cells leads to faster osseointegration, the process in which bone grows onto the implant surface and locks it in place.

If that idea held in practice, the crown could be attached sooner. This is the main reason the surface is promoted as the core of a smart implant.

Some systems are also described as having an antibacterial or tissue-friendly surface that holds fewer bacteria and suits the surrounding soft tissue. The surface of the implant is only one part of the picture around the gum line. Plaque that builds up at the junction between the crown and the gum causes inflammation around implants in much the same way it causes gum disease around natural teeth, and the cleaning routine and regular professional care decide how that area behaves over the years. A surface marketed as antibacterial does not remove the need for that routine.

Whether a surface feature changes outcomes is a question for controlled trials, and for the hydrophilic surface such trials exist.

What Randomised Trials Found About Healing and Survival

The claim of faster healing has been tested directly. A systematic review and meta-analysis pooled 5 randomised controlled trials covering 246 dental implants that compared a hydrophilic surface with a conventional sandblasted, acid-etched surface (PubMed 32450983). Implant stability was measured at baseline and at 3, 6 and 8 weeks, which is the window in which a faster-integrating surface should show its advantage, and survival was recorded as a second outcome (PubMed 32450983). Compared with the conventional surface, the hydrophilic surface showed no clinically significant difference in either implant stability or survival rates (PubMed 32450983).

The authors pointed out that their review had limits: the samples were small and the included studies differed from one another. That caution works in both directions. The data do not prove that the surface is useless, and they do not support the promise that it shortens healing in a way a patient would notice. For now, the healing period before the final crown is decided case by case, from the bone quality, the stability measured at placement and whether grafting was needed.

Longer follow-up of hydrophilic implants is available from smaller series. In a prospective study, 25 hydrophilic bone-level tapered implants were placed immediately after extraction in the back of the mouth in 19 patients, and 24 of the 25 implants (96%) survived for an average of 57 ± 8.07 months (PubMed 38454439). All of the surviving implants were counted as a success, and the most common prosthetic complication was loss of the contact between the crown and the neighbouring tooth, at 41.67% (PubMed 38454439). These are encouraging results for one surface in one setting, without a comparison group.

Digital Planning and Robot-Assisted Placement

The second part of the smart implant package is planning. Before surgery, a three-dimensional scan of the jaw is combined with a digital model of the teeth. Software then places a virtual implant, fixing its position, angle and depth in relation to the bone, the nerve canal, the sinus and the planned crown. The plan is transferred to the mouth either through a printed surgical guide, through a navigation system that tracks the drill in real time, or through a robotic arm.

This part of the technology has a measured error budget. A meta-analysis of 67 articles compared the planned and achieved implant positions and found an overall mean deviation of 1.11 mm at the entry point, 1.40 mm at the apex and 3.51 degrees in angulation (PubMed 38509530). Robot-assisted systems showed the lowest deviations, at 0.81 mm at the entry point, 0.77 mm at the apex and 1.71 degrees in angle (PubMed 38509530). A fully guided protocol was significantly more accurate than a pilot-guided one, in which the guide directs only the first drill (PubMed 38509530).

Digital planning reduces the room for error without bringing it to zero. A deviation of about a millimetre is small in most sites and matters more where the implant sits close to a nerve or a thin wall of bone. For that reason, planned safety margins stay in place even with guided or robotic surgery, and the planning scan is read by the surgeon before the software plan is accepted. Some systems describe their planning as supported by artificial intelligence; the measured accuracy above applies to computer-guided placement in general.

How the Treatment Proceeds

The first visit is a clinical examination with a three-dimensional scan of the jaw. The scan shows the height and width of the bone and the position of structures to avoid, and a digital impression or intraoral scan records the teeth. From these, the implant position is planned and, where a guided protocol is used, a surgical guide is produced.

Placement is carried out under local anaesthesia, so the procedure itself is not painful. Guided surgery can often be done through a small opening in the gum, which limits how much tissue is lifted; the extent of flap elevation is one of the factors behind swelling after surgery. How much discomfort follows varies with the site, the number of implants and whether a tooth was extracted or bone was grafted at the same visit. Mild pain and swelling for a few days is the usual course.

After placement comes the healing period, during which the bone grows onto the implant surface. Its length is set by the surgeon from the stability of the implant and the condition of the bone. Once integration is confirmed, a connecting part called the abutment is attached and a porcelain or zirconia crown is fitted on top. Where biosensor-equipped systems are used, their readings supplement the usual clinical and radiographic follow-up.

Who Is Suitable and Who Should Wait

Suitability for a smart implant is the same as suitability for any dental implant. The surface chemistry and the planning software do not widen the range of patients who can be treated, and they do not remove the reasons for delaying treatment.

The baseline requirements are adequate jawbone volume in the planned site and general health that is under control. Where the bone is too thin or too low, grafting can rebuild it before or during placement, which adds time to the treatment. Patients who have lost teeth and want a fixed replacement, and whose gums are healthy or have been treated, are the usual candidates. Smoking status is assessed as well, because smoking affects healing and is a documented risk factor in related bone procedures; patients who smoke are encouraged to stop, or at least to reduce, before surgery.

Some conditions call for waiting or for a different plan. Patients undergoing chemotherapy or radiotherapy, those with uncontrolled diabetes and those with advanced osteoporosis are the exclusions listed for implant placement, and these remain in place whatever the implant surface. In many cases the barrier is temporary: once cancer treatment is complete, blood sugar is under control or bone medication has been reviewed with the patient's physician, implant treatment can be reassessed.

Active gum disease elsewhere in the mouth is treated before an implant is placed, because the bacteria involved can also inflame the tissue around a new implant.

Brand, Surface and Care Decisions at the Examination

Several implant manufacturers offer a hydrophilic surface as part of their range, and brand is one of the decisions discussed during planning. Brand choice rests on the published data for the specific system, the availability of compatible parts for later repairs and the surgeon's experience with it; the factors involved are covered in more detail in the article on implant brands. A hydrophilic surface can be one reason to choose a system, but given the trial results it is not a reason on its own to expect faster healing or a longer life for the implant.

Warranty terms differ between manufacturers and clinics and should be read in writing before treatment, since they usually cover the implant body and set conditions such as attending check-ups.

The questions answered at the examination are practical ones. Is there enough bone in the planned site, or is grafting needed first? Are there health conditions that need to be controlled before surgery? Which parts of the smart implant package does the proposed system actually use: a hydrophilic surface, fully guided or robot-assisted placement, or sensor follow-up? And how long is the expected healing period for this site, given the bone quality and the stability expected at placement?

Once placed, the life of an implant depends on the same things whatever its surface: daily cleaning around the crown, professional cleaning and regular check-ups at which the gum and the bone level around the implant are examined.

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// Written by
Medically reviewed by: Dr Hakan Kaval
Last updated:

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// Frequently Asked

Frequently asked questions

What is a smart implant in dentistry?+

It is a marketing label rather than a distinct device class. The implant body is still titanium; what differs is the surface treatment, usually a hydrophilic (water-attracting) chemistry that contacts blood and proteins faster than a conventional hydrophobic surface, plus digital planning software that fixes position, angle and depth before surgery. A small number of systems add biosensors intended to let the clinician monitor the implant after placement.

Are smart implants better than conventional implants?+

The controlled evidence does not show a clinically significant advantage. A systematic review and meta-analysis of five randomised trials covering 246 implants compared a hydrophilic surface with a conventional sandblasted, acid-etched surface and found no clinically significant difference in implant stability or survival rates. The authors noted the small sample sizes and differences between the included studies as limitations (PubMed 32450983).

How long does healing take with a smart implant?+

Shorter osseointegration windows are claimed for hydrophilic surfaces than for conventional ones. Controlled evidence does not confirm that shortening: across five randomised trials and 246 implants, implant stability measured at baseline and at 3, 6 and 8 weeks showed no clinically significant difference between hydrophilic and sandblasted, acid-etched surfaces (PubMed 32450983). Healing time is decided case by case.

How accurate is digital implant planning?+

A meta-analysis of 67 clinical studies pooled the deviation between planned and achieved implant position: mean 1.11 mm at the entry point, 95 percent CI 1.02 to 1.19; mean 1.40 mm at the apex; and 3.51 degrees in angulation. Robot-assisted systems showed the lowest deviations at 0.81 mm, 0.77 mm and 1.71 degrees. Fully guided protocols were significantly more accurate than pilot-guided ones (PubMed 38509530).

Is smart implant surgery painful?+

The placement is carried out under local anaesthesia, so the procedure itself is not painful. Discomfort and swelling afterwards vary by case and by how much surgery the site required, including any extraction or grafting performed at the same visit.

Who is not suitable for a dental implant?+

Patients undergoing chemotherapy or radiotherapy, those with uncontrolled diabetes and those with advanced osteoporosis are the exclusions listed for implant placement, and the surface technology does not change them. Adequate jawbone volume and controlled general health are the baseline requirements. Smoking status is assessed as well, since it affects healing and is a documented risk factor in related bone augmentation procedures.

How long do hydrophilic surface implants last?+

Published follow-up is measured in years. In a prospective study of 25 hydrophilic bone-level tapered implants placed immediately in posterior sites in 19 patients, 24 implants (96 percent) survived a mean of 57 plus or minus 8.07 months, roughly four years and nine months, and all surviving implants met the success criteria. Proximal contact loss at 41.67 percent was the most common prosthetic complication (PubMed 38454439).

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