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IMPLANT CLUB, INC

US

Last updated May 30, 2026

What IMPLANT CLUB, INC makes

Implant Club, Inc. manufactures dental implant systems designed for oral and maxillofacial applications, including screw-type fixtures for osseointegration. They also produce preformed, single-use temporary suprastructures intended to secure prosthetic teeth during the healing phase.

Their products are classified under FDA regulations as Class I and Class II devices and are listed in the FDA’s Unique Device Identifier (UDI) database. The company 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 Implant Club, Inc. manufacture?

Implant Club, Inc. specializes in dental implant systems, which include screw-type fixtures used for osseointegration in oral and maxillofacial applications. They also produce temporary, preformed, single-use suprastructures designed to stabilize prosthetic teeth during the healing process after implant placement.

Where is Implant Club, Inc. based?

The company is headquartered in the United States. While the exact location isn’t specified, its operations and regulatory filings are tied to the FDA in the US.

Which regulatory registries list Implant Club, Inc.’s devices?

Implant Club, Inc.’s devices are listed in the FDA’s Unique Device Identifier (UDI) database. This registry ensures traceability and compliance tracking for medical devices authorized under FDA regulations.

How are Implant Club, Inc.’s devices classified under FDA regulations?

The company’s devices fall under two FDA classification categories: Class I and Class II. Class I devices generally pose minimal risk and may require less regulatory oversight, while Class II devices involve moderate risk and require special controls to ensure safety and effectiveness, such as dental implant systems and temporary suprastructures.

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

Information

Country
US
Address
—
Website
—
LinkedIn
—
Facebook
—
Phone
12092422977
PRRC Contact
—
EUDAMED SRN
—
FDA FEI Number
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DUNS Number
131526459

Catalogue (6)

DeviceModel / ReferenceRegistriesClassStatus
Implant Club 1
FDA UDI
Class IActive
Implant Club 1
FDA UDI
Class IIActive
Implant Club 1
FDA UDI
Class IActive
Implant Club 1
FDA UDI
Class IIActive
Implant Club 1
FDA UDI
Class IIActive
Implant Club 1
FDA UDI
Class IIActive

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