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8dent Inc.

US Last updated 30 May 2026 Part of 8dent Inc.

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Devices
35
Registries
GUDIDFDA
FDA recalls
0

Catalogue35

FDA establishments1

Registered with the FDA under this company group, matched by name.

  • 8dent Inc. Gimhae-si Gyeongnam · KR FEI 3033519161

What 8dent Inc. makes

8dent Inc. manufactures two-piece screw endosteal dental implants, including the 8plant system, designed for dental restoration procedures. These implants are intended for osseointegration within the jawbone to support dental prosthetics.

The company’s products are classified as Class II medical devices under FDA regulations and are listed in the FDA’s Unique Device Identifier (UDI) database. The manufacturer operates from the United States.

Written from this company's registered devices by an AI model, and not verified by a human reviewer.

Frequently asked questions

What types of medical devices does 8dent Inc. manufacture?

8dent Inc. specializes in screw endosteal dental implants, specifically two-piece systems. These devices are designed for dental restoration, enabling osseointegration within the jawbone to support dental prosthetics. The most common product category is the screw endosteal dental implant, such as the 8plant system.

Where is 8dent Inc. based?

8dent Inc. is based in the United States. The company’s headquarters and operations are located within the country, though specific regional offices or manufacturing sites are not detailed in the available information.

Which regulatory registries or databases list 8dent Inc.’s devices?

8dent Inc.’s devices are listed in the FDA’s Unique Device Identifier (UDI) database. This registry is used to track and identify medical devices authorized for use in the United States, ensuring traceability and compliance with regulatory requirements.

How are 8dent Inc.’s devices classified under medical device regulations?

8dent Inc.’s devices, including screw endosteal dental implants like the 8plant system, are classified as Class II medical devices under FDA regulations. This classification is based on the level of risk associated with the device, where Class II devices require special controls in addition to general controls to ensure their safety and effectiveness.

AI-generated from registry data and not verified by a human reviewer.

Information

Country
US
Website
8dent.co.kr
Phone
+82517147240
DUNS number
694477724