MIS SEVEN

Also known as: SEVEN, MIS Seven implant

A root-shaped bone-level implant from MIS on the internal hexagon platform, with micro-rings at the neck and a dome-shaped apex.

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Quick facts

Manufacturer	MIS Implants Technologies Ltd.Manufacturer-reported[1]
Implant level	Bone levelManufacturer-reported[1]
Body geometry	Root-shaped geometry with micro-rings on the neck of the implantManufacturer-reported[1]
Thread design	Thread design described by MIS as unique to SEVEN and intended for primary stabilityManufacturer-reported[1]
Apex design	Dome-shaped apex, which MIS states prevents over-insertionManufacturer-reported[1]
Material	Titanium alloy Ti-6Al-4V ELIManufacturer-reported[1]
Surface	Sandblasted and acid-etchedManufacturer-reported[1]
Connection	Internal hexagon, shared with the M4 implant across narrow, standard and wide platformsManufacturer-reported[1][2]
Platform switching	Manufacturer documentation not located
Available diameters	Ø3.30, 3.75, 4.20, 5.00 and 6.00 mmManufacturer-reported[1]
Available lengths	Ø3.30 in 10, 11.5, 13 and 16 mm; Ø3.75 in 8, 10, 11.5, 13 and 16 mm; Ø4.20 and Ø5.00 in 6, 8, 10, 11.5, 13 and 16 mm; Ø6.00 in 6, 8, 10, 11.5 and 13 mmManufacturer-reported[1]

Overview

SEVEN sits on the internal hexagon platform, which is the older of the two MIS families and is entirely separate from the conical connection used by C1 and V3 — components do not cross between them. Within its own family it shares a connection with M4, so those two are restoratively interchangeable. The dome-shaped apex is a deliberate safety feature rather than a stability one: a blunt tip is less likely to be driven past the intended depth. SEVEN reaches Ø6.00 mm, the widest fixture MIS lists on this platform.

Further detail

Geographic availability	Requires manual verification

Clinical evidence

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

Similar implant systems

Popular comparisons

MIS C1 vs SEVEN

The clearances below are held by MIS at brand level and cover its implant range, not MIS SEVEN 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 SEVEN Product Catalog — Internal Hexagon — MIS Implants Technologies Ltd.. Accessed 2026-07-21.
[2]Internal Hexagon Product Catalog 2025 — MIS Implants Technologies Ltd., 2025. Accessed 2026-07-21.