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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 26 of 36
DeviceModel / ReferenceRegistriesClassStatus
Bite Impression Coping OBICR4003
FDA UDI
Class IActive
Transfer Impression Coping OSICT4516N
FDA UDI
Class IActive
Solid Abutment OSSA4075T
FDA UDI
Class IIActive
Healing Abutment OSHAM4007G
FDA UDI
Class IIActive
Fixture POF5013QNP
FDA UDI
Class IIActive
Bite Scan Body OBICR5502SBP
FDA UDI
Class IActive
Bite Scan Body OBICM4003SBP
FDA UDI
Class IActive
Transfer Impression Coping OSICTM4014NP
FDA UDI
Class IActive
Hex Driver OMDSS1200
FDA UDI
Class IActive
Cemented Abutment OSCA5042NP
FDA UDI
Class IIActive
Healing Abutment OSHA4005G
FDA UDI
Class IIActive
Pick-Up Impression Coping PIIC4808
FDA UDI
Class IActive
Solid Abutment OSSA5052
FDA UDI
Class IIActive
Transfer Impression Coping OSICT7016NP
FDA UDI
Class IActive
Solid Abutment OSSAM4045
FDA UDI
Class IIActive
Final Drill OTFD4013
FDA UDI
Class IActive
Pick-Up Impression Coping PIICP4812NP
FDA UDI
Class IActive
Solid Abutment OSSAM4552
FDA UDI
Class IIActive
Cemented Abutment OSCA6073HTP
FDA UDI
Class IIActive
Bite Impression Coping OBICR4502P
FDA UDI
Class IActive
Transfer Impression Coping OSICT6014H
FDA UDI
Class IActive
Transfer Impression Coping OSICT4514N
FDA UDI
Class IActive
Transfer Impression Coping OSICTM4016N
FDA UDI
Class IActive
Abutment Removal Tip OSARMTS
FDA UDI
Class IActive
Solid Abutment OSSA4545T
FDA UDI
Class IIActive
Solid Abutment OSSA4043T
FDA UDI
Class IIActive
Cemented Abutment OSCA5072N
FDA UDI
Class IIActive
Guide Pin PIGP2014
FDA UDI
Class IActive
Transfer Impression Coping OSICT6511H
FDA UDI
Class IActive
Cemented Abutment OSCA6043NT
FDA UDI
Class IIActive
Fixture POF7007Q
FDA UDI
Class IIActive
Fixture POF5008
FDA UDI
Class IIActive
Pick-Up Impression Coping OSICP6017NP
FDA UDI
Class IActive
Plastic Sleeve OSPC4500N
FDA UDI
Class IActive
Transfer Impression Coping OSICT5514N
FDA UDI
Class IActive
Cemented Abutment OSCA6045NT
FDA UDI
Class IIActive
Solid Abutment OSSA4052T
FDA UDI
Class IIActive
Solid Abutment OSSAM4542
FDA UDI
Class IIActive
Scan Body OSBM
FDA UDI
Class IActive
Bite Scan Body OBICR4006SB
FDA UDI
Class IActive
Bite Scan Body OBICR4004SBP
FDA UDI
Class IActive
Slot Driver OMDSS0500
FDA UDI
Class IActive
Bite Scan Body OBICR4504SBP
FDA UDI
Class IActive
Final Drill OTFDA3510
FDA UDI
Class IActive
Transfer Impression Coping OSICT5511NP
FDA UDI
Class IActive
Cemented Abutment OSCA6045H
FDA UDI
Class IIActive
Final Drill OTFDA5008
FDA UDI
Class IActive
Angled Abutment OSAAM4504NT
FDA UDI
Class IIActive
Pick-up Impression Coping OSICPM4017H
FDA UDI
Class IActive
Cemented Abutment OSCA5075HT
FDA UDI
Class IIActive

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