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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 30 of 36
DeviceModel / ReferenceRegistriesClassStatus
Solid Abutment OSSA6072TP
FDA UDI
Class IIActive
Solid Abutment OSSA4045T
FDA UDI
Class IIActive
Solid Abutment OSSA4543
FDA UDI
Class IIActive
Solid Abutment OSSA4541TP
FDA UDI
Class IIActive
Cemented Abutment OSCA4555HT
FDA UDI
Class IIActive
Fixture POF5007QNP
FDA UDI
Class IIActive
Solid Abutment OSSA4044P
FDA UDI
Class IIActive
Cemented Abutment OSCAM4555HT
FDA UDI
Class IIActive
Solid Abutment OSSAM4051
FDA UDI
Class IIActive
Impression Coping Driver OBICDL
FDA UDI
Class IActive
Cemented Abutment OSCAM4555H
FDA UDI
Class IIActive
Cortical Drill OTCD5500
FDA UDI
Class IActive
Solid Abutment OSSA4053TP
FDA UDI
Class IIActive
Transfer Impression Coping OSICT4016NP
FDA UDI
Class IActive
Cemented Abutment OSCA4553N
FDA UDI
Class IIActive
Cemented Abutment OSCA5071NT
FDA UDI
Class IIActive
Transfer Impression Coping OSICT4511HP
FDA UDI
Class IActive
Fixture Driver OFDTC2100S
FDA UDI
Class IActive
Cemented Abutment OSCA5043N
FDA UDI
Class IIActive
Cemented Abutment OSCA5071HTP
FDA UDI
Class IIActive
Cemented Abutment OSCAM4551HT
FDA UDI
Class IIActive
Solid Abutment OSSAM4571P
FDA UDI
Class IIActive
Fixture Driver OFDT2500
FDA UDI
Class IActive
Solid Abutment OSSA5074TP
FDA UDI
Class IIActive
Bite Impression Coping OBICM4504
FDA UDI
Class IActive
Bite Impression Coping OBICR4508
FDA UDI
Class IActive
Temporary Abutment OSTAM4030N
FDA UDI
Class IIActive
Final Drill NFD4010
FDA UDI
Class IActive
Pick-Up Impression Coping OSICP5517N
FDA UDI
Class IActive
Pick-Up Impression Coping PIICP4807
FDA UDI
Class IActive
Bite Scan Body OBICM4008SB
FDA UDI
Class IActive
Transfer Impression Coping OSICT6511NP
FDA UDI
Class IActive
Pick-Up Impression Coping PIIC4808P
FDA UDI
Class IActive
Cemented Abutment OSCA6051H
FDA UDI
Class IIActive
Transfer Impression Coping OSICTX4014N
FDA UDI
Class IActive
Solid Abutment OSSA4574TP
FDA UDI
Class IIActive
Solid Abutment OSSA5075P
FDA UDI
Class IIActive
Cemented Abutment OSCA4552HTP
FDA UDI
Class IIActive
Solid Abutment OSSAM4543TP
FDA UDI
Class IIActive
Cemented Abutment OSCA6042HTP
FDA UDI
Class IIActive
Fixture POF4507QNP
FDA UDI
Class IIActive
Solid Abutment OSSA4545
FDA UDI
Class IIActive
Solid Abutment OSSA5041TP
FDA UDI
Class IIActive
Pick-Up Impression Coping OSICP5515NP
FDA UDI
Class IActive
Mount Open Wrench OSOW
FDA UDI
Class IActive
Cemented Abutment OSCA6045HP
FDA UDI
Class IIActive
Cemented Abutment OSCAM4554H
FDA UDI
Class IIActive
Fixture POF3513QNP
FDA UDI
Class IIActive
Fixture Pin PIFP3500
FDA UDI
Class IActive
Final Drill NFD4511
FDA UDI
Class IActive

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