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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 27 of 36
DeviceModel / ReferenceRegistriesClassStatus
Solid Abutment OSSA6041T
FDA UDI
Class IIActive
Solid Abutment OSSA4054T
FDA UDI
Class IIActive
Cemented Abutment OSCA7054HT
FDA UDI
Class IIActive
Cemented Abutment OSCA6041H
FDA UDI
Class IIActive
Solid Abutment OSSA5055TP
FDA UDI
Class IIActive
Solid Abutment OSSA4572TP
FDA UDI
Class IIActive
Angled Abutment OSAA5002NT
FDA UDI
Class IIActive
Solid Abutment OSSA6075P
FDA UDI
Class IIActive
Bite Scan Body OBICR4508SB
FDA UDI
Class IActive
Transfer Impression Coping OSICT5016H
FDA UDI
Class IActive
Bite Impression Coping OBICR5006P
FDA UDI
Class IActive
Solid Abutment OSSA6055T
FDA UDI
Class IIActive
Transfer Impression Coping OSICT5511H
FDA UDI
Class IActive
Plastic Sleeve OIPC4800N
FDA UDI
Class IActive
Pick-Up Impression Coping OSICP7011H
FDA UDI
Class IActive
Angled Abutment OSAA6004AP
FDA UDI
Class IIActive
Solid Abutment OSSA4051
FDA UDI
Class IIActive
Solid Abutment OSSA6043TP
FDA UDI
Class IIActive
Impression Coping Driver OBICHS
FDA UDI
Class IActive
Cemented Abutment OSCA5052N
FDA UDI
Class IIActive
Cemented Abutment OSCA5042N
FDA UDI
Class IIActive
Tissue Punch Drill NTPD3440
FDA UDI
Class IActive
Ball Analog OSBLA400
FDA UDI
Class IActive
Pick-Up Impression Coping OSICPX4011HP
FDA UDI
Class IActive
Solid Abutment OSSAM4045TP
FDA UDI
Class IIActive
Cemented Abutment OSCA5055HT
FDA UDI
Class IIActive
Solid Abutment OSSA4072T
FDA UDI
Class IIActive
Bite Scan Body OBICR7002SB
FDA UDI
Class IActive
Solid Abutment OSSA6044P
FDA UDI
Class IIActive
Solid Abutment OSSAM4073TP
FDA UDI
Class IIActive
Pick-Up Impression Coping OSICP4017NP
FDA UDI
Class IActive
Solid Abutment OSSA4054TP
FDA UDI
Class IIActive
Cemented Abutment OSCAM4552NT
FDA UDI
Class IIActive
Final Drill OTFDA4008
FDA UDI
Class IActive
Cemented Abutment OSCA7053H
FDA UDI
Class IIActive
Angled Abutment OSAA5004NT
FDA UDI
Class IIActive
Angled Abutment OSAAM4502AP
FDA UDI
Class IIActive
Cemented Abutment OSCA4552HP
FDA UDI
Class IIActive
Guide Pin OBICS2006
FDA UDI
Class IActive
Fixture POF5011
FDA UDI
Class IIActive
Guide Drill OGD1900
FDA UDI
Class IActive
Bite Scan Body OBICR5008SB
FDA UDI
Class IActive
Solid Abutment OSSAM4553
FDA UDI
Class IIActive
Bite Scan Body OBICR4506SBP
FDA UDI
Class IActive
Cemented Abutment OSCA7055NP
FDA UDI
Class IIActive
Solid Abutment OSSA6071TP
FDA UDI
Class IIActive
Pro-Kit PRO-KIT
FDA UDI
Class IActive
Pick-Up Impression Coping OSICP7015N
FDA UDI
Class IActive
Bite Scan Body OBICM4006SB
FDA UDI
Class IActive
Transfer Impression Coping OSICT5011H
FDA UDI
Class IActive

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