Implant system · MegaGen

MegaGen AnyRidge

Partially verifiedLast verified 27 Sept 2026 · data version 1

Quick answer

MegaGen AnyRidge is a dental implant system from MegaGen (MegaGen Implant Co., Ltd.). It is made of commercially pure titanium, grade 4 with a Xpeed® surface and uses a internal hex (octa variant: anyridge octa 1) connection. We link 3 FDA 510(k) records to this system. Open any value below to see its source.

Brand and system alone do not decide how an implant does. Bone, gum health, smoking, the surgeon's skill, the restoration and maintenance all matter. How to compare implant systems →

Manufacturer

Brand
MegaGen
Manufacturer (regulatory name)
MegaGen Implant Co., Ltd.
Headquarters country
South Korea (headquarters, not necessarily the place of manufacture)
Status
Currently marketed
Also known as
AnyRidge, Any Ridge, Xpeed AnyRidge, AnyRidge Octa 1

Implant type

Implant levelWhere the top of the implant sits: level with the bone, or higher up in the gum.
Two-stage root-form fixture (bone level)
Regulatory record1 source · verified 27 Sept 2026
Body shapeThe overall shape of the screw that goes into the jaw.
Tapered body
Regulatory record1 source · verified 27 Sept 2026

Material & surface

MaterialWhat the implant screw itself is made of.
Commercially pure titanium, grade 4
Regulatory record2 sources · verified 27 Sept 2026
Material grade
SurfaceHow the outer surface is treated so bone can grow onto it.
Xpeed® — SLA-type surface; manufacturer describes hydrothermal calcium-ion incorporation
Manufacturer-stated
FDA K140091 describes the surface treatment as SLA; the calcium modification is the manufacturer's description.
Regulatory recordManufacturer documentation2 sources · verified 27 Sept 2026

Connection

ConnectionHow the visible tooth part (abutment) attaches to the implant.
Internal hex (Octa variant: AnyRidge Octa 1)
Taper angle of the internal connection not yet confirmed from a MegaGen primary technical document.
Regulatory record2 sources · verified 27 Sept 2026
Connection angleNot verified
Anti-rotation indexNot verified
Prosthetic platformsNot verified

Size range

DiametersHow thick the implant is. Your dentist chooses based on your bone.
Normal ridge Ø4.0, 4.4, 4.9, 5.4, 5.9 mm; low ridge Ø6.4, 6.9, 7.4, 7.9, 8.4 mm (2014 FDA summary)
Later Octa 1 clearance (K182448) adds narrower diameters from Ø3.6 mm. Current global catalogue pending.
Regulatory record1 source · verified 27 Sept 2026
LengthsHow long the implant is. Shorter ones are used where there is less bone.
Normal ridge 7.7, 9.2, 10.7, 12.2, 14.2, 17.2 mm; low ridge 7.9–14.4 mm (2014 FDA summary)
Regulatory record1 source · verified 27 Sept 2026

Macrogeometry · technical detail for dentists

Thread design
KnifeThread® — self-tapping, knife-shaped progressive thread
Manufacturer-stated
Manufacturer documentation1 source · verified 27 Sept 2026
ApexNot verified
Neck / collarNot verified

Indications

Immediate function (labeling)Whether a temporary tooth may be fitted on the same day, according to official labeling.
What the regulatory labeling permits. It is not evidence that immediate loading works better with this system.
US labeling (2014): implants < Ø6.0 mm for immediate loading with good primary stability; larger implants for molar region with delayed loading
Regulatory record1 source · verified 27 Sept 2026
Restrictions & cautionsNot verified

Surgical protocol · technical detail for dentists

Max insertion torqueNot verified

Regulatory records

RecordDevice name (as filed)ApplicantDecisionDate
K110955AnyRidge Internal Implant SystemMegagen Co., Ltd.Substantially Equivalent22 Nov 2011
K140091Xpeed AnyRidge Internal Implant SystemMegagen Implant Co., Ltd.Substantially Equivalent12 Dec 2014
K182448AnyRidge Octa 1 Implant SystemMegagen Implant Co., Ltd.Substantially Equivalent9 Oct 2019

FDA clearance means the FDA found the device substantially equivalent to a legally marketed device. It is not a ranking of quality or clinical results. EU (EUDAMED) records will be added.

Safety notices & recalls

No FDA recall record found.

openFDA recall search “product_description:AnyRidge” run on 27 Sept 2026: 0 result(s). No result is not proof that no recall or field safety notice exists in any market.

Clinical evidence

We have not yet linked any system-specific studies to MegaGen AnyRidge. Evidence on materials, connections and loading protocols that applies across systems is in the evidence explorer. We don't quote single-study survival rates as brand scores.

Compare AnyRidge with…

Sources

  1. FDA 510(k) K140091 — Xpeed AnyRidge Internal Implant System (510(k) summary) — U.S. Food and Drug Administration, 2014-12-12. Accessed 27 Sept 2026.
  2. FDA 510(k) K182448 — AnyRidge Octa 1 Implant System (510(k) summary) — U.S. Food and Drug Administration, 2019-10-09. Accessed 27 Sept 2026.
  3. AnyRidge® — product page — MegaGen Implant Co., Ltd.. Accessed 27 Sept 2026.
  4. openFDA Device 510(k) API — U.S. Food and Drug Administration. Accessed 27 Sept 2026.

MegaGen, AnyRidge, Xpeed and KnifeThread are trademarks of MegaGen Implant Co., Ltd. Found an error? Email info@dentalimplantbrands.com.

Educational information only. Implant-system selection requires assessment by a qualified dental professional.

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