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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 35 of 36
DeviceModel / ReferenceRegistriesClassStatus
Transfer Impression Coping OSICT5011N
FDA UDI
Class IActive
Plastic Sleeve OSPC3500H
FDA UDI
Class IActive
Bite Impression Coping OBICR4004
FDA UDI
Class IActive
Initial Drill NID3011
FDA UDI
Class IActive
Solid Abutment OSSA7053TP
FDA UDI
Class IIActive
Bite Scan Body OBICR4503SBP
FDA UDI
Class IActive
Bite Impression Coping OBICR6004P
FDA UDI
Class IActive
Cemented Abutment OSCA5075NP
FDA UDI
Class IIActive
Transfer Impression Coping OSICT6516H
FDA UDI
Class IActive
Solid Abutment OSSAM4073
FDA UDI
Class IIActive
Solid Abutment OSSAM4051P
FDA UDI
Class IIActive
Cemented Abutment OSCA5044H
FDA UDI
Class IIActive
Final Drill OTFD4513N
FDA UDI
Class IActive
Solid Abutment OSSAM4552TP
FDA UDI
Class IIActive
Bite Impression Coping OBICM4002P
FDA UDI
Class IActive
Solid Abutment OSSA6042T
FDA UDI
Class IIActive
Pick-Up Impression Coping OSICP5015HP
FDA UDI
Class IActive
Cemented Abutment OSCA6052NT
FDA UDI
Class IIActive
Cemented Abutment OSCA6052HT
FDA UDI
Class IIActive
Fixture POF6010QNP
FDA UDI
Class IIActive
Navi-Kit NAVI-KIT
FDA UDI
Class IActive
Bite Impression Coping OBICR4006
FDA UDI
Class IActive
Guide Drill OGD1900S
FDA UDI
Class IActive
Solid Abutment OSSA6053
FDA UDI
Class IIActive
Bite Scan Body OBICR6004SB
FDA UDI
Class IActive
Cemented Abutment OSCA6044N
FDA UDI
Class IIActive
Solid Abutment OSSA6055P
FDA UDI
Class IIActive
Cemented Abutment OSCA5042HTP
FDA UDI
Class IIActive
Solid Abutment OSSA4044T
FDA UDI
Class IIActive
Cemented Abutment OSCA5043NP
FDA UDI
Class IIActive
Final Drill NFD4513
FDA UDI
Class IActive
Cemented Abutment OSCAM4554NP
FDA UDI
Class IIActive
Bite Impression Coping OBICR4008P
FDA UDI
Class IActive
Cemented Abutment OSCA5054NT
FDA UDI
Class IIActive
Cemented Abutment OSCA6055NP
FDA UDI
Class IIActive
Bite Impression Coping OBICR5508P
FDA UDI
Class IActive
Angled Abutment OSAA5004BTP
FDA UDI
Class IIActive
Solid Abutment OSSA4541P
FDA UDI
Class IIActive
Bite Scan Body OBICR5002SB
FDA UDI
Class IActive
Cemented Abutment OSCA6051HP
FDA UDI
Class IIActive
Pick-Up Impression Coping OSICPM4015H
FDA UDI
Class IActive
Solid Abutment OSSA4554
FDA UDI
Class IIActive
Pick-Up Impression Coping OSICP4511NP
FDA UDI
Class IActive
Cemented Abutment OSCA5055NP
FDA UDI
Class IIActive
Solid Abutment OSSA4071T
FDA UDI
Class IIActive
Transfer Impression Coping OSICT6016NP
FDA UDI
Class IActive
Cover screw OCS3500G
FDA UDI
Class IIActive
Slot Driver OTDL0600
FDA UDI
Class IActive
Bite Impression Coping OBICM4502P
FDA UDI
Class IActive
Bite Impression Coping OBICR5502
FDA UDI
Class IActive

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