MIS M4
Also known as: M4, MIS M4 implant
A bone-level implant from MIS on the internal hexagon platform, sharing its connection with SEVEN and differing in external geometry.
Research in progress. Some fields on this entry are not yet verified against a primary source, so we have left them blank rather than filling them in — and this page is not published to search engines until they are.
Quick facts
| Manufacturer | MIS Implants Technologies Ltd.Manufacturer-reported[1] |
|---|---|
| Implant level | Bone levelManufacturer-reported[1] |
| Body geometry | Manufacturer documentation not located |
| Thread design | Manufacturer documentation not located |
| Apex design | Manufacturer documentation not located |
| Material | Titanium alloy Ti-6Al-4V ELIManufacturer-reported[1] |
| Surface | Manufacturer documentation not located(MIS describes a sandblasted and acid-etched surface across its implants generally; we have not located a statement specific to M4.) |
| Connection | Internal hexagon, the same platform used by SEVEN, on narrow, standard and wide platformsManufacturer-reported[1] |
| 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]Read from the product codes in the 2025 internal hexagon catalogue. |
Overview
Further detail
| Geographic availability | Requires manual verification |
|---|
Clinical evidence
We have not yet completed a system-specific evidence review for MIS M4. Insufficient system-specific evidence How we grade evidence
Similar implant systems
The clearances below are held by MIS at brand level and cover its implant range, not MIS M4 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]Internal Hexagon Product Catalog 2025 — MIS Implants Technologies Ltd., 2025. Accessed 2026-07-21.