Implance Short Implant

Also known as: Implance Short

The short-implant option within the Turkish Implance system, in bone-level and tissue-level forms for reduced bone height.

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Quick facts

Manufacturer	AGS Medikal (Implance)Manufacturer-reported[1]
Body geometry	Short fixtures offered in both bone-level and tissue-level forms for cases where bone height is limitedManufacturer-reported[1]
Material	Manufacturer documentation not located
Surface	RBM (Resorbable Blasting Media) roughened surfaceManufacturer-reported[3][1]
Connection	Internal 11-degree conical (Morse-taper) connectionManufacturer-reported[2][1]
Available diameters	Ø4.3, Ø4.8 and Ø5.5 mmManufacturer-reported[1]
Available lengths	Bone level: 5.0 and 6.0 mm; tissue level: 4.0, 5.0 and 6.0 mmManufacturer-reported[1]

Overview

The Implance short implant is offered for situations where the sinus above or the nerve below leaves too little bone height for a conventional fixture, so a wider, shorter implant is used instead of grafting. It comes in both bone-level and tissue-level forms, with lengths down to 4–6 mm. Short implants are a well-recognised category with their own evidence base; the value of this record is simply that Implance offers the option, in the widths and lengths the catalogue documents.

Technology

BrandImplance

Clinical evidence

We have not yet completed a system-specific evidence review for Implance Short Implant. Insufficient system-specific evidence How we grade evidence

Similar implant systems

The clearances below are held by Implance at brand level and cover its implant range, not Implance Short Implant specifically. We show them here because that is the level at which regulators actually issue them.

Regulatory record

Read this before drawing conclusions. A clearance or certificate means a device may legally be sold in a market. It is not a finding that the implant performs well, and it is not a comparison against other implants. In particular, FDA "clearance" is not FDA "approval" — clearance means the FDA accepted the device as substantially equivalent to one already on the market. What these actually mean →

FDA 510(k) clearance1 record

Cleared as substantially equivalent to a predicate device. Not an FDA approval, and not a finding of safety or effectiveness.

Number	Device	Holder	Date
K160221	Implance Dental Implant System, Implance Dental Abutment System	Ags Medikal Urunleri Ith. Ihr. Tic. Ltd. Sti.	2016-09-12

Clearance records for Implance were retrieved from the issuing authority's own database, not from the manufacturer's marketing material. We attribute a clearance to a brand only when the filing holder belongs to that brand's corporate family — third-party clearances for compatible components are excluded, because they belong to the company that made the component, not to Implance.

Sources

Numbers match the citations beside each claim above.

Primary sources

[1]Implance Dental Implant System — Catalogue (EN) — AGS Medikal Ürünleri İth. İhr. Tic. A.Ş.. Accessed 2026-07-22.
[2]Design Specifications — Implance — AGS Medikal Ürünleri İth. İhr. Tic. A.Ş.. Accessed 2026-07-22.
[3]Surface Specifications — Implance — AGS Medikal Ürünleri İth. İhr. Tic. A.Ş.. Accessed 2026-07-22.