IDIS

Also known as: S-Plant

The implant brand of IDIS Co., Ltd. of South Korea, whose product is the S-Plant dental implant system.

Key facts

Manufacturer	IDIS Co., Ltd.Verified spec[1]
Country	South KoreaVerified spec[1]
Surface	SLA (sandblasted with large grit, acid-etched) on grade-4 commercially pure titaniumVerified spec[1]
Connection	Tapered conical-hex connectionVerified spec[1]
manufacturingCountry	South KoreaVerified spec[2]Country of the FDA-registered device establishment, which may differ from the brand’s home country.

Overview

IDIS is a smaller Korean brand whose single FDA-cleared product is S-Plant, a grade-4 titanium fixture with an SLA surface and a tapered conical-hex connection. It is not widely distributed internationally, and there is little English-language material beyond its regulatory filing, so this record is intentionally narrow.

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 →

FDA 510(k) clearance1 record

Cleared as substantially equivalent to a predicate device. Not an FDA approval, and not a finding of safety or effectiveness.

Number	Device	Holder	Date
K231429	S-Plant Dental Implant System	Idis Co., Ltd.	2023-12-18

Other1 record

Registered device establishment in South Korea. 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
3026365523	—	IDIS CO., LTD.	—

Clearance records for IDIS 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 IDIS.

Sources

Numbers match the citations beside each claim above.

Primary sources

[1]FDA 510(k) K221866 — S-Plant Dental Implant System — U.S. Food & Drug Administration, 2023. Accessed 2026-07-21.
[2]openFDA — Device registrations and listings — US Food and Drug Administration. Accessed 2026-07-22.