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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 12 of 36
DeviceModel / ReferenceRegistriesClassStatus
Cemented Abutment OSCA6055HT
FDA UDI
Class IIActive
Final Drill OTFDA7007
FDA UDI
Class IActive
Pick-Up Impression Coping OSICP7017H
FDA UDI
Class IActive
Cemented Abutment OSCA6053NP
FDA UDI
Class IIActive
Solid Abutment OSSAM4072T
FDA UDI
Class IIActive
Multi Abutment Carrier OMCR4800
FDA UDI
Class IActive
Bite Scan Body OBICR5003SBP
FDA UDI
Class IActive
Final Drill OTFDA6513
FDA UDI
Class IActive
Cemented Abutment OSCA4554NP
FDA UDI
Class IIActive
Cemented Abutment OSCAM4554NT
FDA UDI
Class IIActive
Angled Abutment OSAAM4504NP
FDA UDI
Class IIActive
Impression Coping Driver OBICHL
FDA UDI
Class IActive
Cemented Abutment OSCA5053N
FDA UDI
Class IIActive
Cemented Abutment OSCAM4553H
FDA UDI
Class IIActive
Solid Abutment OSSAM4551P
FDA UDI
Class IIActive
Solid Abutment OSSAM4075TP
FDA UDI
Class IIActive
Solid Abutment OSSAM4575P
FDA UDI
Class IIActive
Bite Scan Body OBICR5506SB
FDA UDI
Class IActive
Pick-Up Impression Coping OSICP4017N
FDA UDI
Class IActive
Final Drill OTFD7013
FDA UDI
Class IActive
Transfer Impression Coping PIICT6512
FDA UDI
Class IActive
Cemented Abutment OSCA5054HP
FDA UDI
Class IIActive
Transfer Impression Coping PIICT6512N
FDA UDI
Class IActive
Temporary Abutment OSTA4530H
FDA UDI
Class IIActive
Fixture Mount Screw OFMRS
FDA UDI
Class IActive
Angled Abutment OSAA6002A
FDA UDI
Class IIActive
Bite Impression Coping OBICR6003P
FDA UDI
Class IActive
Transfer Impression Coping OSICT4011NP
FDA UDI
Class IActive
Solid Abutment OSSA5045TP
FDA UDI
Class IIActive
Fixture POF4007
FDA UDI
Class IIActive
Solid Abutment OSSAM4071TP
FDA UDI
Class IIActive
Angled Abutment OSAA5002AT
FDA UDI
Class IIActive
Angled Abutment OSAAM4504N
FDA UDI
Class IIActive
Bite Impression Coping OBICM4503P
FDA UDI
Class IActive
Solid Driver ORDS4000
FDA UDI
Class IActive
Temporary Abutment OSTAM4030H
FDA UDI
Class IIActive
Angled Abutment OSAAM4502AT
FDA UDI
Class IIActive
Cemented Abutment OSCA4551HTP
FDA UDI
Class IIActive
Solid Abutment OSSAM4542TP
FDA UDI
Class IIActive
Solid Abutment OSSA7055P
FDA UDI
Class IIActive
Pick-Up Impression Coping OSICPM4015NP
FDA UDI
Class IActive
Solid Abutment OSSA6051T
FDA UDI
Class IIActive
Cemented Abutment OSCA6055N
FDA UDI
Class IIActive
Solid Abutment OSSA5052TP
FDA UDI
Class IIActive
Solid Abutment OSSAM4041
FDA UDI
Class IIActive
Solid Abutment OSSA4055
FDA UDI
Class IIActive
Solid Abutment OSSA4043
FDA UDI
Class IIActive
Final Drill OTFDA5013
FDA UDI
Class IActive
Bite Impression Coping OBICR4506
FDA UDI
Class IActive
Solid Abutment OSSA5042T
FDA UDI
Class IIActive

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