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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 18 of 36
DeviceModel / ReferenceRegistriesClassStatus
Transfer Impression Coping OSICT4016H
FDA UDI
Class IActive
Slot Driver OTDS0500
FDA UDI
Class IActive
Bite Impression Coping OBICM4008
FDA UDI
Class IActive
Solid Abutment OSSA5044TP
FDA UDI
Class IIActive
Final Drill NFD5007
FDA UDI
Class IActive
Solid Abutment OSSA4051TP
FDA UDI
Class IIActive
Pick-Up Impression Coping OSICPX4015H
FDA UDI
Class IActive
Cemented Abutment OSCAM4551HP
FDA UDI
Class IIActive
Final Drill OTFD6013
FDA UDI
Class IActive
Fixture POF6008Q
FDA UDI
Class IIActive
Cemented Abutment OSCA7054N
FDA UDI
Class IIActive
Pick-Up Impression Coping PIIC4812P
FDA UDI
Class IActive
Cemented Abutment OSCA5055N
FDA UDI
Class IIActive
Cemented Abutment OSCA6052H
FDA UDI
Class IIActive
Transfer Impression Coping OSICTX4014HP
FDA UDI
Class IActive
Cemented Abutment OSCA4553HTP
FDA UDI
Class IIActive
Scan Body OSBR
FDA UDI
Class IActive
Hex Driver OMDL1200
FDA UDI
Class IActive
Final Drill OTFDA3513
FDA UDI
Class IActive
Final Drill OTFDA6006
FDA UDI
Class IActive
Pick-Up Impression Coping OSICP5017N
FDA UDI
Class IActive
Initial Drill NID2213
FDA UDI
Class IActive
Transfer Impression Coping OSICTM4516NP
FDA UDI
Class IActive
Bite Impression Coping OBICM4004
FDA UDI
Class IActive
Fixture Driver OFDTC2100EL
FDA UDI
Class IActive
Solid Abutment OSSAM4075T
FDA UDI
Class IIActive
Cemented Abutment OSCA6054NT
FDA UDI
Class IIActive
Final Drill NFD3510
FDA UDI
Class IActive
Bite-Kit BITE-KIT
FDA UDI
Class IActive
Plastic Sleeve OSPC3500N
FDA UDI
Class IActive
Cemented Abutment OSCA5073N
FDA UDI
Class IIActive
Fixture Driver NFD25R
FDA UDI
Class IActive
Solid Abutment OSSAM4545P
FDA UDI
Class IIActive
Solid Abutment OSSAM4074TP
FDA UDI
Class IIActive
Solid Abutment OSSA6071
FDA UDI
Class IIActive
Bite Impression Coping OBICR5008P
FDA UDI
Class IActive
Fixture POF6007Q
FDA UDI
Class IIActive
Cemented Abutment OSCA5054HTP
FDA UDI
Class IIActive
Solid Abutment OSSA4041
FDA UDI
Class IIActive
Cemented Abutment OSCA5054HT
FDA UDI
Class IIActive
Cemented Abutment OSCA5044NT
FDA UDI
Class IIActive
Bite Impression Coping OBICR4503
FDA UDI
Class IActive
Cortical Drill OTCD4000
FDA UDI
Class IActive
Cemented Abutment OSCA7052NP
FDA UDI
Class IIActive
Solid Abutment OSSA4055TP
FDA UDI
Class IIActive
Cemented Abutment OSCA6055NT
FDA UDI
Class IIActive
Bite Scan Body OBICM4004SB
FDA UDI
Class IActive
Pick-Up Impression Coping OSICP4015H
FDA UDI
Class IActive
Cemented Abutment OSCAM4554N
FDA UDI
Class IIActive
Transfer Impression Coping OSICTX4016HP
FDA UDI
Class IActive

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