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CONELOG PROGRESSIVE-LINE

Also known as: CONELOG Progressive-Line, PROGRESSIVE-LINE

A CAMLOG implant in grade 4 titanium with a partly conical body and a 7.5 degree conical implant-abutment connection with three grooves, supplied with the Promote plus surface.

Quick facts

Current statusCurrent. CAMLOG publishes a CONELOG PROGRESSIVE-LINE work instruction dated 2019.Manufacturer-reported[1]
Implant levelManufacturer documentation not located(CAMLOG states the implant can be placed both epicrestally and subcrestally, and does not classify it by level.)
Body geometryA body combining a parallel-walled section with a progressive apical form, developed for high initial stability; CAMLOG also offers a reduced diameter for areas with little bone.Manufacturer-reported[1]
Thread designManufacturer documentation not located(The work instruction describes the implant as designed for high initial stability but does not give a thread pitch specification.)
Apex designApical diameter ∅ 2.7 mm for the ∅ 3.3, 3.8 and 4.3 mm implants and ∅ 3.2 mm for the ∅ 5.0 mm implant.Manufacturer-reported[1]
MaterialTitanium grade 4. Abutments and abutment screws are Ti6Al4V ELI.Manufacturer-reported[1]
SurfacePromote plus — an abrasive-blasted, acid-etched surface extending over the implant body to the acid-etched implant shoulder.Manufacturer-reported[1]
ConnectionA 7.5° cone with three grooves in the inner configuration. CONELOG abutments carry a matching cone and three cams which lock into the grooves, giving a rotation-locked connection.Manufacturer-reported[1]
Platform switchingIntegrated platform switching — CAMLOG states the CONELOG abutment does not cover the implant shoulder.Manufacturer-reported[1]
Available diameters∅ 3.3, 3.8, 4.3 and 5.0 mm, colour-coded grey, yellow, red and blue.Manufacturer-reported[1]
Available lengths9, 11, 13 and 16 mm for the ∅ 3.3 mm implant; 7, 9, 11, 13 and 16 mm for ∅ 3.8, 4.3 and 5.0 mm.Manufacturer-reported[1]

Overview

CONELOG PROGRESSIVE-LINE is the conical-connection half of CAMLOG’s range, and the connection is the whole point of the distinction: a 7.5° cone with three grooves and matching cams, rather than the cylindrical Tube-in-Tube used by CAMLOG SCREW-LINE. Because the abutment does not cover the implant shoulder, platform switching is built into the geometry rather than being an optional component choice. The PROGRESSIVE-LINE body differs from the older CONELOG SCREW-LINE in its apical form, which CAMLOG developed for higher initial stability in immediate and early protocols. One point worth carrying into a consultation: CAMLOG restricts the 7 mm length to specific conditions set out in its own instructions, so a 7 mm CONELOG is not simply a shorter option freely available at any site.

Technology

Clinical positioning

What the manufacturer says this system is designed for. This is not the same thing as independent clinical evidence, which is set out separately below.

CAMLOG states the implant can be placed epicrestally or subcrestally, is suitable for late as well as more immediate protocols, and cautions that 7 mm implants should only be used under the conditions set out in the work instruction.Manufacturer-reported

Further detail

Narrow implant optionCAMLOG describes the ∅ 3.3 mm implant as an alternative for areas with little bone.Manufacturer-reported[1]

Clinical evidence

We have not yet completed a system-specific evidence review for CONELOG PROGRESSIVE-LINE. Insufficient system-specific evidence How we grade evidence

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Popular comparisons

The clearances below are held by CAMLOG at brand level and cover its implant range, not CONELOG PROGRESSIVE-LINE 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 →

Other1 record

Registered device establishment in Switzerland. Registration records where a device is made or handled; it is not a clearance, an approval, or any assessment of the product.

NumberDeviceHolderDate
3007283751CAMLOG Biotechnologies GmbH

Clearance records for CAMLOG 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 CAMLOG.

Sources

Numbers match the citations beside each claim above.

Primary sources

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