MIS C1

Also known as: C1, C1 XD, MIS C1 implant

A conical, root-shaped bone-level implant from MIS with a dual thread and a 12-degree friction-fit conical connection with platform switching.

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Quick facts

Manufacturer	MIS Implants Technologies Ltd.Manufacturer-reported[1]
Implant level	Bone levelManufacturer-reported[1]
Body geometry	Conical, root-shaped geometry with micro-rings on the implant neckManufacturer-reported[1]
Thread design	Dual thread designManufacturer-reported[1]
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-switching designManufacturer-reported[1]
Available diameters	Ø3.30 mm on the narrow platform; Ø3.75 and Ø4.20 mm on the standard platform; Ø5.00 mm on the wide platformManufacturer-reported[1]
Available lengths	Ø3.30 in 10, 11.5, 13 and 16 mm; Ø3.75, Ø4.20 and Ø5.00 in 8, 10, 11.5, 13 and 16 mmManufacturer-reported[1]

Overview

C1 is the conventional counterpart to V3: a round, root-shaped tapered implant on the same 12-degree conical connection, so the two can be mixed within a case and restored with identical components. Current MIS literature labels it C1 XD, where the XD refers to the single-use drill protocol supplied with each implant rather than to a change in the implant itself. The micro-rings on the neck and the platform-switched connection are both aimed at the crestal bone, which is where most measurable bone change happens in the first year.

Further detail

Prosthetic ecosystem	Shares the MIS conical connection prosthetic range with V3; supplied with single-use XD drillsManufacturer-reported[1]
Geographic availability	Requires manual verification

Clinical evidence

We have not yet completed a system-specific evidence review for MIS C1. Insufficient system-specific evidence How we grade evidence

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The clearances below are held by MIS at brand level and cover its implant range, not MIS C1 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 C1 XD Product Catalog — Conical Connection — MIS Implants Technologies Ltd.. Accessed 2026-07-21.