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MegaGen AnyRidge

Also known as: AnyRidge, AnyRidge Internal

A tapered bone-level implant from MegaGen built around a knife-edge thread, in which the thread depth changes across the range while the core diameter stays the same.

Quick facts

ManufacturerMegaGen Implant Co., Ltd.Manufacturer-reported[1][2]
Body geometryTapered fixture in which several fixture diameters share a single core diameter, so the drilling sequence is chosen by bone type rather than by fixture widthManufacturer-reported[1][3]
Thread designKnifeThread — MegaGen describes it as a self-tapping knife-shaped progressive thread with variable thread depths at the same core diameter, intended to ease insertion, leave space for blood supply and increase surface areaManufacturer-reported[1]This is MegaGen’s own wording; the thread is the defining feature of the design.
Apex designNarrow apical diameter, specified as 1.6 mm at Ø3.5, 1.8 mm from Ø4.0 to Ø5.5 and 3.0 mm from Ø6.0 to Ø8.0Manufacturer-reported[3]
MaterialManufacturer documentation not located(The AnyRidge catalogue does not state a titanium grade for the fixture.)
SurfaceXPEED — MegaGen describes a hydro-thermal incorporation of calcium ions producing a calcium titanate nanostructure on the surfaceManufacturer-reported[1]The XPEED surface is also the subject of independent laboratory and animal work.
ConnectionInternal connection combining a 5-degree Morse taper with a 2.3 mm internal hex, the same size on every fixture diameterManufacturer-reported[3]
Platform switchingThe platform diameter is narrower than the widest thread diameter on every size, and MegaGen presents 0.5 to 1.0 mm subcrestal placement as the intended positionManufacturer-reported[3]
Available diametersTen fixture diameters: Ø3.5, 4.0, 4.5, 5.0, 5.5, 6.0, 6.5, 7.0, 7.5 and 8.0 mm, built on core diameters of 3.3, 3.8, 4.0, 4.3 and 4.8 mmManufacturer-reported[3]
Available lengths7, 8.5, 10, 11.5, 13 and 15 mm; the 7 mm option is subject to local approval and the widest fixtures are not offered at 15 mmManufacturer-reported[3]

Overview

AnyRidge is defined by its thread rather than its body: MegaGen keeps the core of the implant the same and varies how far the knife-shaped thread projects, so a Ø5.0 fixture and a Ø4.0 fixture can be prepared through a similar osteotomy and the surgeon selects width by bone quality. That is why MegaGen’s literature talks about core diameters and fixture diameters as separate numbers, and why the ten-diameter range is smaller in practice than it looks. The surface, XPEED, is a calcium-ion treatment rather than a plain blasted and etched finish, and it is specific to MegaGen. The connection is a shallow 5-degree taper with an internal hex, identical on every diameter, which is what makes one set of prosthetic parts serve the whole range.

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.

Presented for a wide range of bone types, with the drilling sequence chosen by bone density rather than by fixture diameterManufacturer-reported

Further detail

Geographic availabilityRequires manual verification

Clinical evidence

We have not yet completed a system-specific evidence review for MegaGen AnyRidge. Insufficient system-specific evidence How we grade evidence

Similar implant systems

Popular comparisons

The clearances below are held by MegaGen at brand level and cover its implant range, not MegaGen AnyRidge 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) clearance8 records

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

NumberDeviceHolderDate
K251232MegaGen Zygoma Dental Implant SystemMegagen Implant Co., Ltd.2026-06-18
K242030MegaGen Dental Implant AbutmentMegagen Implant Co., Ltd.2025-01-13
K233450MegaGen Dental Implant Abutment - Scan Healing Abutment; Temporary Abutment; Temporary Cylinder; Comfort Cap; Healing Cap; Healing Cap Screw; Milling Abutment; EZ Post Abutment; Extra EZ Post Abutment; EZ Post Cylinder; ZrGEN Abutment; Multi-unit Abutment; Multi-unit Angled Abutment; AXA Abutment (Straight); AXA Abutment (Angled); Abutment Screw; Cylinder Screw; Crown ScrewMegagen Implant Co., Ltd.2024-01-22
K230618MegaGen Dental Implant Systems Portfolio - MR ConditionalMegagen Implant Co., Ltd.2023-10-11
K182448AnyRidge Octa 1 Implant SystemMegagen Implant Co., Ltd.2019-10-09
K140091XPEED ANYRIDGE INTERNAL IMPLANT SYSYEMMegagen Implant Co., Ltd.2014-12-12
K123870XPEED ANYRIDGE INTERNAL IMPLANT SYSTEMMegagen Implant Co., Ltd.2013-03-27
K110955ANYRIDGE INTERNAL IMPLANT SYSTEMMegagen Co., Ltd.2011-11-22

Other3 records

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

NumberDeviceHolderDate
3030089802MegaGen Implant Co., Ltd. (Research Laboratories)
3005554774Megagen Implant Co., Ltd.
1332 device recordsMegaGen

Clearance records for MegaGen 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 MegaGen.

Sources

Numbers match the citations beside each claim above.

Primary sources

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