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.
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 | Grade 4 Regulatory record2 sources · verified 27 Sept 2026 |
| 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 angle | Not verified |
| Anti-rotation index | Not verified |
| Prosthetic platforms | Not 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 |
|---|---|
| Apex | Not verified |
| Neck / collar | Not 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 & cautions | Not verified |
Surgical protocol · technical detail for dentists
| Max insertion torque | Not verified |
|---|
Regulatory records
| Record | Device name (as filed) | Applicant | Decision | Date |
|---|---|---|---|---|
| K110955 | AnyRidge Internal Implant System | Megagen Co., Ltd. | Substantially Equivalent | 22 Nov 2011 |
| K140091 | Xpeed AnyRidge Internal Implant System | Megagen Implant Co., Ltd. | Substantially Equivalent | 12 Dec 2014 |
| K182448 | AnyRidge Octa 1 Implant System | Megagen Implant Co., Ltd. | Substantially Equivalent | 9 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
- 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.
- 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.
- AnyRidge® — product page — MegaGen Implant Co., Ltd.. Accessed 27 Sept 2026.
- 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.