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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 11 of 36
DeviceModel / ReferenceRegistriesClassStatus
Guide Pin OBICS1603
FDA UDI
Class IActive
Fixture Driver OFDT2100S
FDA UDI
Class IActive
Bite Scan Body OBICR7003SBP
FDA UDI
Class IActive
Solid Abutment OSSAM4042
FDA UDI
Class IIActive
Cemented Abutment OSCA5045N
FDA UDI
Class IIActive
Bite Impression Coping OBICR7006
FDA UDI
Class IActive
Pick-Up Impression Coping OSICP5517HP
FDA UDI
Class IActive
Fixture POF4010QNP
FDA UDI
Class IIActive
Fixture Driver OFDT2500EL
FDA UDI
Class IActive
Cemented Abutment OSCA7053NTP
FDA UDI
Class IIActive
Bite Impression Coping OBICR7008P
FDA UDI
Class IActive
Solid Driver OSDL
FDA UDI
Class IActive
Solid Abutment OSSAM4051T
FDA UDI
Class IIActive
Cemented Abutment OSCA6073NTP
FDA UDI
Class IIActive
Cemented Abutment OSCA4551HT
FDA UDI
Class IIActive
Pick-Up Impression Coping OSICPX4517H
FDA UDI
Class IActive
Initial Drill NID3008
FDA UDI
Class IActive
Ball Abutment Driver OBDT2400S
FDA UDI
Class IActive
Fixture POF7008QNP
FDA UDI
Class IIActive
Fixture Pin OSFPRS
FDA UDI
Class IActive
Pick-Up Impression Coping OSICP4015N
FDA UDI
Class IActive
Final Drill OTFDA6008
FDA UDI
Class IActive
Pick-Up Impression Coping OSICP6517H
FDA UDI
Class IActive
Impression Coping Driver OBICDS
FDA UDI
Class IActive
Transfer Impression Coping OSICTM4514N
FDA UDI
Class IActive
Solid Abutment OSSAM4054
FDA UDI
Class IIActive
Final Drill NFD3511
FDA UDI
Class IActive
Transfer Impression Coping OSICT4511NP
FDA UDI
Class IActive
Parallel Pin OPP6000
FDA UDI
Class IActive
Bite Scan Body OBICR5503SBP
FDA UDI
Class IActive
Final Drill OTFDA5011
FDA UDI
Class IActive
Final Drill OTFD3507
FDA UDI
Class IActive
Solid Abutment OSSA4071P
FDA UDI
Class IIActive
Solid Abutment OSSA5051P
FDA UDI
Class IIActive
Pick-Up Impression Coping OSICPM4511NP
FDA UDI
Class IActive
Bite Impression Coping OBICR6004
FDA UDI
Class IActive
Cemented Abutment OSCA5043NTP
FDA UDI
Class IIActive
Pick-Up Impression Coping OSICPX4517NP
FDA UDI
Class IActive
Solid Abutment OSSA5074P
FDA UDI
Class IIActive
Cemented Abutment OSCA4555N
FDA UDI
Class IIActive
Cemented Abutment OSCA5073HT
FDA UDI
Class IIActive
Cemented Abutment OSCA6075H
FDA UDI
Class IIActive
Angled Abutment OSAAM4504A
FDA UDI
Class IIActive
Bite Impression Coping OBICR5008
FDA UDI
Class IActive
Initial Drill NID2207
FDA UDI
Class IActive
Final Drill OTFD4507
FDA UDI
Class IActive
Bite Impression Coping OBICR7008
FDA UDI
Class IActive
Cemented Abutment OSCA4553H
FDA UDI
Class IIActive
Fixture POF4008QNP
FDA UDI
Class IIActive
Transfer Impression Coping OSICT4014HP
FDA UDI
Class IActive

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