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MegaGen

Also known as: MegaGen Implant, AnyRidge

The South Korean implant brand behind the AnyRidge, AnyOne and BlueDiamond implant systems.

Research in progress. Some fields on this entry are not yet verified against a primary source, so we have left them blank rather than filling them in — and this page is not published to search engines until they are.

Key facts

ManufacturerMegaGen Implant Co., Ltd.Verified spec[1]
Parent companyMegaGen Implant Co., Ltd.Verified spec[1]
CountrySouth KoreaVerified spec[1]
HeadquartersDaegu, South KoreaVerified spec[1]
FoundedManufacturer documentation not located(Frequently reported as 2002, but not stated on the manufacturer pages we reached)
Manufacturer-described indicationAnyRidge is presented as a biologically inspired design supporting immediate placement and loading; BlueDiamond is presented as the premium system for digital workflowsManufacturer-reported[1]
manufacturingCountrySouth KoreaVerified spec[2]Country of the FDA-registered device establishment, which may differ from the brand’s home country.

Overview

MegaGen is a Korean brand that appears regularly in treatment quoted abroad, usually as AnyRidge. AnyRidge, AnyOne, BlueDiamond and ARi are separate implant designs rather than trim levels of one product, and a treatment plan naming only “MegaGen” has not identified which one was used. This record is database-only because the manufacturer’s own pages do not give a founding date, and we have not established the company’s ownership structure — both are things a reader would reasonably expect on a manufacturer profile, and we would rather leave them empty than borrow them from a directory listing.

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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