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POINTIMPLANT Co., Ltd.

US

Last updated May 29, 2026

Part of POINTIMPLANT Co., Ltd

What POINTIMPLANT Co., Ltd. makes

PointImplant Co., Ltd. manufactures dental implant components, including permanent and temporary preformed suprastructures, single-use precision attachments for scanning and simulation, and reusable dental drill bits. Their portfolio also covers two-piece endosteal dental implants, reusable abutment screw analogs, and intraoral-scanning abutment analogs. Surgical screwdrivers and healing abutments are also part of their product range.

The company’s devices are classified under FDA regulations as Class I and Class II, with all products listed in the FDA’s Unique Device Identifier (UDI) database. These items are intended for dental applications and are subject to compliance with U.S. medical device regulations.

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 PointImplant Co., Ltd. manufacture?

PointImplant Co., Ltd. specializes in dental implant components and related accessories. Their products include permanent and temporary preformed suprastructures for dental implants, single-use precision attachments like scanning simulators and intraoral-scanning abutment analogs, reusable dental drill bits, and two-piece endosteal dental implants. They also produce reusable tools such as surgical screwdrivers and abutment screw analogs, as well as healing abutments. These devices are designed to support dental restoration procedures.

Where is PointImplant Co., Ltd. based, and what regulatory database lists their devices?

PointImplant Co., Ltd. is based in the United States. Their devices are listed in the FDA’s Unique Device Identifier (UDI) database, which is a central registry for tracking medical devices authorized for use in the U.S. This database helps ensure transparency and traceability of their products under FDA regulations.

How are PointImplant Co., Ltd.’s devices classified under FDA regulations?

PointImplant Co., Ltd.’s devices are classified under the FDA’s medical device regulations as either Class I or Class II. The classification depends on factors like the device’s intended use, potential risks, and the body’s interaction with it. For example, reusable tools like drill bits and screwdrivers are typically Class II due to their critical role in surgical precision, while some single-use components may fall under Class I if they pose lower risk. Classification determines the regulatory pathway for authorization.

What does it mean for PointImplant Co., Ltd.’s devices to be listed in the FDA’s UDI database?

Listing in the FDA’s Unique Device Identifier (UDI) database means that each of PointImplant Co., Ltd.’s devices has been assigned a unique code to ensure traceability and identification throughout their lifecycle. This system helps healthcare providers, regulators, and manufacturers track devices for safety monitoring, recalls, and compliance with U.S. medical device laws. It also supports transparency in the supply chain, ensuring that only authorized products enter the market.

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

Information

Country
US
Address
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Website
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LinkedIn
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Facebook
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Email
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Phone
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PRRC Contact
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EUDAMED SRN
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FDA FEI Number
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DUNS Number
695333960

Catalogue (1771)

Page 13 of 36
DeviceModel / ReferenceRegistriesClassStatus
Final Drill OTFD7008
FDA UDI
Class IActive
Solid Abutment OSSAM4552T
FDA UDI
Class IIActive
Cemented Abutment OSCA6071N
FDA UDI
Class IIActive
Fixture POF6008QNP
FDA UDI
Class IIActive
Fixture POF4010
FDA UDI
Class IIActive
Pick-Up Impression Coping OSICPX4511NP
FDA UDI
Class IActive
Fixture POF7010
FDA UDI
Class IIActive
Cemented Abutment OSCA4554NTP
FDA UDI
Class IIActive
Cemented Abutment OSCA5051HTP
FDA UDI
Class IIActive
Solid Abutment OSSA5071T
FDA UDI
Class IIActive
Bite Impression Coping OBICM4508
FDA UDI
Class IActive
Cemented Abutment OSCA4553HP
FDA UDI
Class IIActive
Initial Drill OID2715
FDA UDI
Class IActive
Cortical Drill OTCD7000
FDA UDI
Class IActive
Final Drill OTFD6008
FDA UDI
Class IActive
Solid Abutment OSSAM4542T
FDA UDI
Class IIActive
Cemented Abutment OSCA4552NT
FDA UDI
Class IIActive
Solid Abutment OSSA5044T
FDA UDI
Class IIActive
Bite Impression Coping OBICR4504P
FDA UDI
Class IActive
Fixture POF7007QNP
FDA UDI
Class IIActive
Bite Impression Coping OBICR5504
FDA UDI
Class IActive
Solid Abutment OSSA5055T
FDA UDI
Class IIActive
Cemented Abutment OSCA6074HT
FDA UDI
Class IIActive
Pick-Up Impression Coping OSICPM4515HP
FDA UDI
Class IActive
Final Drill OTFD5008
FDA UDI
Class IActive
Solid Abutment OSSA5071
FDA UDI
Class IIActive
Solid Abutment OSSA6052P
FDA UDI
Class IIActive
Pick-Up Impression Coping OSICPM4517N
FDA UDI
Class IActive
Cemented Abutment OSCA5074HTP
FDA UDI
Class IIActive
Sidecut Drill OSCD3000
FDA UDI
Class IActive
Solid Abutment OSSA6075
FDA UDI
Class IIActive
Bite Impression Coping OBICR7006P
FDA UDI
Class IActive
Solid Abutment OSSA6055TP
FDA UDI
Class IIActive
Cemented Abutment OSCA6072NTP
FDA UDI
Class IIActive
Transfer Impression Coping OSICT4014H
FDA UDI
Class IActive
Cemented Abutment OSCA5043H
FDA UDI
Class IIActive
Fixture POF5013Q
FDA UDI
Class IIActive
Solid Abutment OSSAM4573TP
FDA UDI
Class IIActive
Cemented Abutment OSCAM4551HTP
FDA UDI
Class IIActive
Healing Abutment OSHA6007G
FDA UDI
Class IIActive
Mount Extension OMETL
FDA UDI
Class IActive
Cemented Abutment OSCA7055NTP
FDA UDI
Class IIActive
Pick-Up Impression Coping OSICP4515NP
FDA UDI
Class IActive
Fixture POF7008
FDA UDI
Class IIActive
Slot Driver OMDS0600
FDA UDI
Class IActive
Cemented Abutment OSCA6054HTP
FDA UDI
Class IIActive
Cemented Abutment OSCA6055H
FDA UDI
Class IIActive
Guide pin OSICTML
FDA UDI
Class IActive
Cemented Abutment OSCA6042HT
FDA UDI
Class IIActive
Fixture POF4513
FDA UDI
Class IIActive

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