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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)

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DeviceModel / ReferenceRegistriesClassStatus
Cap OSSPC604
FDA UDI
Class IIActive
Scan Body Screw ISBSS
FDA UDI
Class IActive
Solid Abutment OSSAM4543
FDA UDI
Class IIActive
Pick-Up Impression Coping OSICP4511H
FDA UDI
Class IActive
Solid Abutment OSSA4575T
FDA UDI
Class IIActive
Bite Impression Coping OBICR6008
FDA UDI
Class IActive
Cemented Abutment OSCA5051NTP
FDA UDI
Class IIActive
Solid Abutment OSSAM4044
FDA UDI
Class IIActive
Pick-Up Impression Coping PIICP6512
FDA UDI
Class IActive
Healing Abutment OSHA4003G
FDA UDI
Class IIActive
Cemented Abutment OSCA5045HT
FDA UDI
Class IIActive
Angled Abutment OSAA5004N
FDA UDI
Class IIActive
Hex driver OHDS1200
FDA UDI
Class IActive
Solid Abutment OSSAM4571
FDA UDI
Class IIActive
Fixture analog OSTLA400
FDA UDI
Class IActive
Transfer Impression Coping OSICT7011H
FDA UDI
Class IActive
Solid Abutment OSSA7055
FDA UDI
Class IIActive
Solid Abutment OSSA6044
FDA UDI
Class IIActive
Transfer Impression Coping OSICT5014N
FDA UDI
Class IActive
Solid Abutment OSSAM4075
FDA UDI
Class IIActive
Abutment Removal Tip OSARMTEL
FDA UDI
Class IActive
Final Drill OTFD5013N
FDA UDI
Class IActive
Solid Abutment OSSA7054TP
FDA UDI
Class IIActive
Fixture POF4511QNP
FDA UDI
Class IIActive
Pick-Up Impression Coping OSICPM4011HP
FDA UDI
Class IActive
Cemented Abutment OSCA6053H
FDA UDI
Class IIActive
Cemented Abutment OSCA5071NP
FDA UDI
Class IIActive
Cemented Abutment OSCA6051N
FDA UDI
Class IIActive
Transfer Impression Coping OSICT6514NP
FDA UDI
Class IActive
Solid Abutment OSSA6054T
FDA UDI
Class IIActive
Cemented Abutment OSCA6043NP
FDA UDI
Class IIActive
Point Drill NPD2705
FDA UDI
Class IActive
Cortical Drill OTCD6000
FDA UDI
Class IActive
Cemented Abutment OSCA5075NT
FDA UDI
Class IIActive
Hex Driver OTSDL1200
FDA UDI
Class IActive
Hex Driver OHDS1207
FDA UDI
Class IActive
Removal Tool ORTM
FDA UDI
Class IActive
Solid Abutment OSSA4575TP
FDA UDI
Class IIActive
Solid Abutment OSSA4551P
FDA UDI
Class IIActive
Solid Abutment OSSA4544P
FDA UDI
Class IIActive
Fixture POF3508Q
FDA UDI
Class IIActive
Cemented Abutment OSCA6051HTP
FDA UDI
Class IIActive
Transfer Impression Coping OSICTX4016N
FDA UDI
Class IActive
Slot Driver OMDL0600
FDA UDI
Class IActive
Final Drill OTFDA4506
FDA UDI
Class IActive
Solid Abutment OSSA4555T
FDA UDI
Class IIActive
Fixture POF4510
FDA UDI
Class IIActive
Cemented Abutment OSCA6074H
FDA UDI
Class IIActive
Cemented Abutment OSCA5041H
FDA UDI
Class IIActive
Solid Abutment OSSA7051TP
FDA UDI
Class IIActive

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