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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 33 of 36
DeviceModel / ReferenceRegistriesClassStatus
Cemented Abutment OSCA5044HTP
FDA UDI
Class IIActive
Cemented Abutment OSCA6044H
FDA UDI
Class IIActive
Final Drill OTFD3513N
FDA UDI
Class IActive
Solid Abutment OSSAM4571T
FDA UDI
Class IIActive
Osteotome OSTM
FDA UDI
Class IActive
Solid Abutment OSSA4055P
FDA UDI
Class IIActive
Healing Abutment OSHA7003G
FDA UDI
Class IIActive
Transfer Impression Coping OSICTX4516HP
FDA UDI
Class IActive
Angled Abutment OSAA6004ATP
FDA UDI
Class IIActive
Transfer Impression Coping OSICT6514H
FDA UDI
Class IActive
Solid Abutment OSSA7053P
FDA UDI
Class IIActive
Fixture POF4011Q
FDA UDI
Class IIActive
Solid Abutment OSSAM4074P
FDA UDI
Class IIActive
Temporary Abutment OSTAM4010NP
FDA UDI
Class IIActive
Bite Impression Coping OBICR5503P
FDA UDI
Class IActive
Cemented Abutment OSCA5052HT
FDA UDI
Class IIActive
Solid Abutment OSSA6073
FDA UDI
Class IIActive
Solid Abutment OSSAM4553TP
FDA UDI
Class IIActive
Bite Scan Body OBICR6004SBP
FDA UDI
Class IActive
Bite Scan Body OBICR5506SBP
FDA UDI
Class IActive
Cemented Abutment OSCA4555NP
FDA UDI
Class IIActive
Bite Scan Body OBICM4008SBP
FDA UDI
Class IActive
Cemented Abutment OSCA6051NT
FDA UDI
Class IIActive
Cover screw OCS3000G
FDA UDI
Class IIActive
Bite Scan Body OBICR4502SB
FDA UDI
Class IActive
Pick-Up Impression Coping PIICP4812N
FDA UDI
Class IActive
Cemented Abutment OSCA6052N
FDA UDI
Class IIActive
Pick-up Impression Coping OSICP7011N
FDA UDI
Class IActive
Cemented Abutment OSCA6074NP
FDA UDI
Class IIActive
Pick-Up Impression Coping OSICP6517NP
FDA UDI
Class IActive
Solid Abutment OSSA4042P
FDA UDI
Class IIActive
Cemented Abutment OSCA6071H
FDA UDI
Class IIActive
Healing Abutment OSHA6005G
FDA UDI
Class IIActive
Cemented Abutment OSCA6052HTP
FDA UDI
Class IIActive
Angled Abutment OSAA6004BT
FDA UDI
Class IIActive
Solid Abutment OSSA7055T
FDA UDI
Class IIActive
Guide pin OSICTS
FDA UDI
Class IActive
Cemented Abutment OSCAM4553NTP
FDA UDI
Class IIActive
Solid Abutment OSSA6042TP
FDA UDI
Class IIActive
Cemented Abutment OSCA7051NTP
FDA UDI
Class IIActive
Pick-Up Impression Coping OSICP6011NP
FDA UDI
Class IActive
Cemented Abutment OSCA6044HT
FDA UDI
Class IIActive
Solid Abutment OSSA5043P
FDA UDI
Class IIActive
Angled Abutment OSAA6002B
FDA UDI
Class IIActive
Solid Abutment OSSAM4575TP
FDA UDI
Class IIActive
Solid Abutment OSSA5071P
FDA UDI
Class IIActive
Pick-Up Impression Coping OSICP5511NP
FDA UDI
Class IActive
Transfer Impression Coping OSICT6014N
FDA UDI
Class IActive
Fixture Driver NFDM21M
FDA UDI
Class IActive
Pick-Up Impression Coping OSICPM4017N
FDA UDI
Class IActive

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