MIS V3

Also known as: V3, MIS V3 implant

A bone-level implant from MIS with a triangular coronal section and a 12-degree friction-fit conical connection, made in titanium alloy with a blasted and acid-etched surface.

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Quick facts

Manufacturer	MIS Implants Technologies Ltd.Manufacturer-reported[1]
Implant level	Bone levelManufacturer-reported[1]
Body geometry	Triangular-shaped coronal neck, which MIS states is intended to create gaps around the implant neck for blood pooling and clot formationManufacturer-reported[1]
Thread design	Manufacturer documentation not located
Apex design	Manufacturer documentation not located
Material	Titanium alloy Ti-6Al-4V ELIManufacturer-reported[1]
Surface	Sandblasted and acid-etchedManufacturer-reported[1]
Connection	12-degree friction-fit conical connectionManufacturer-reported[1]
Platform switching	Platform-switched designManufacturer-reported[1]
Available diameters	Ø3.30 mm on the narrow platform; Ø3.90, Ø4.30 and Ø5.00 mm on the standard platformManufacturer-reported[1]
Available lengths	Ø3.30 in 10, 11.5, 13 and 16 mm; Ø3.90, Ø4.30 and Ø5.00 in 8, 10, 11.5, 13 and 16 mmManufacturer-reported[1]

Overview

V3 is the unusual one in the MIS range: the coronal third of the implant is triangular in cross-section rather than round, so that when it is seated there are three small voids between implant and bone. MIS’s stated reasoning is that those spaces fill with blood and then bone, and that the reduced contact reduces compression at the crest. Whether that produces a measurable clinical difference is a separate question from whether the geometry is real — the geometry certainly is. V3 and C1 share the same 12-degree conical connection and prosthetic components, so they are interchangeable on the restorative side.

Further detail

Immediate protocol	Maximum placement torque of 45 Ncm at Ø3.30 and 60 Ncm at Ø3.90Manufacturer-reported[1]
Prosthetic ecosystem	Shares the MIS conical connection prosthetic range with C1; each package includes a sterile single-use final drillManufacturer-reported[1]
Geographic availability	Requires manual verification

Clinical evidence

We have not yet completed a system-specific evidence review for MIS V3. Insufficient system-specific evidence How we grade evidence

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Popular comparisons

MIS V3 vs C1

The clearances below are held by MIS at brand level and cover its implant range, not MIS V3 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 →

Other2 records

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

Number	Device	Holder	Date
3004203816	—	MIS Implants Technologies Ltd.	—
446 device records	—	MIS	—

Clearance records for MIS 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 MIS.

Sources

Numbers match the citations beside each claim above.

Primary sources

[1]MIS V3 Product Catalog — Conical Connection — MIS Implants Technologies Ltd.. Accessed 2026-07-21.