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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 5 of 36
DeviceModel / ReferenceRegistriesClassStatus
Solid Abutment OSSAM4044T
FDA UDI
Class IIActive
Pick-Up Impression Coping OSICPX4011NP
FDA UDI
Class IActive
Solid Abutment OSSA4573T
FDA UDI
Class IIActive
Cemented Abutment OSCA6072NP
FDA UDI
Class IIActive
Solid Abutment OSSA4053
FDA UDI
Class IIActive
Solid Abutment OSSA4051T
FDA UDI
Class IIActive
Cemented Abutment OSCA4551HP
FDA UDI
Class IIActive
Pick-Up Impression Coping OSICP7011NP
FDA UDI
Class IActive
Fixture POF3511QNP
FDA UDI
Class IIActive
Cemented Abutment OSCA6045N
FDA UDI
Class IIActive
Solid Abutment OSSA5055
FDA UDI
Class IIActive
Solid Abutment OSSAM4573T
FDA UDI
Class IIActive
Solid Abutment OSSA4573P
FDA UDI
Class IIActive
Fixture POF5013
FDA UDI
Class IIActive
Bite Impression Coping OBICM4008P
FDA UDI
Class IActive
Abutment Removal Tip OSARTS
FDA UDI
Class IActive
Transfer Impression Coping PIICT6509NP
FDA UDI
Class IActive
Solid Abutment OSSAM4545T
FDA UDI
Class IIActive
Cemented Abutment OSCA5074NP
FDA UDI
Class IIActive
Cemented Abutment OSCAM4551NTP
FDA UDI
Class IIActive
Solid Abutment OSSA5073T
FDA UDI
Class IIActive
Abutment Removal Tip OSARTL
FDA UDI
Class IActive
Fixture POF3508QNP
FDA UDI
Class IIActive
Bite Impression Coping OBICR4008
FDA UDI
Class IActive
Initial Drill NID2210
FDA UDI
Class IActive
Fixture POF3510
FDA UDI
Class IIActive
Angled Abutment OSAAM4502BTP
FDA UDI
Class IIActive
Temporary Abutment OSTA4510HP
FDA UDI
Class IIActive
Angled Abutment OSAA6002NT
FDA UDI
Class IIActive
Cemented Abutment OSCA5045H
FDA UDI
Class IIActive
Solid Abutment OSSAM4552P
FDA UDI
Class IIActive
Angled Abutment OSAA5004AP
FDA UDI
Class IIActive
Transfer Impression Coping OSICT4016HP
FDA UDI
Class IActive
Cemented Abutment OSCA7053NT
FDA UDI
Class IIActive
Cemented Abutment OSCA7053HT
FDA UDI
Class IIActive
Scan Body Screw OSBRS
FDA UDI
Class IActive
Solid Abutment OSSA4541
FDA UDI
Class IIActive
Fixture POF7013
FDA UDI
Class IIActive
Cemented Abutment OSCA5052NTP
FDA UDI
Class IIActive
Transfer Impression Coping OSICTM4014N
FDA UDI
Class IActive
Cemented Abutment OSCAM4551NT
FDA UDI
Class IIActive
Bite Impression Coping OBICM4006
FDA UDI
Class IActive
Solid Abutment OSSA7052T
FDA UDI
Class IIActive
Healing Abutment OSHAM4505G
FDA UDI
Class IIActive
Cemented Abutment OSCA5071NTP
FDA UDI
Class IIActive
Solid Abutment OSSA5075TP
FDA UDI
Class IIActive
Bite Impression Coping OBICR4502
FDA UDI
Class IActive
Cortical Drill OTCD3500
FDA UDI
Class IActive
Solid Abutment OSSA4053P
FDA UDI
Class IIActive
Cemented Abutment OSCA6075NP
FDA UDI
Class IIActive

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