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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 7 of 36
DeviceModel / ReferenceRegistriesClassStatus
Fixture POF6013
FDA UDI
Class IIActive
Bite Scan Body OBICR6003SBP
FDA UDI
Class IActive
Pick-Up Impression Coping OSICPX4011H
FDA UDI
Class IActive
Solid Abutment OSSA4044TP
FDA UDI
Class IIActive
Cemented Abutment OSCA7051NT
FDA UDI
Class IIActive
Cemented Abutment OSCAM4555HP
FDA UDI
Class IIActive
Cemented Abutment OSCA7053HTP
FDA UDI
Class IIActive
Bite Impression Coping OBICR4002P
FDA UDI
Class IActive
Fixture Driver OFDH2500S
FDA UDI
Class IActive
Solid Abutment OSSA7052TP
FDA UDI
Class IIActive
Solid Abutment OSSA5041T
FDA UDI
Class IIActive
Transfer Impression Coping OSICT7011N
FDA UDI
Class IActive
Bite Scan Body OBICR4008SBP
FDA UDI
Class IActive
Cemented Abutment OSCA5075H
FDA UDI
Class IIActive
Solid Abutment OSSAM4544
FDA UDI
Class IIActive
Bite Scan Body OBICR5004SBP
FDA UDI
Class IActive
Solid Abutment OSSA6054TP
FDA UDI
Class IIActive
Angled Abutment OSAA6002BTP
FDA UDI
Class IIActive
Cemented Abutment OSCA7053NP
FDA UDI
Class IIActive
Pick-Up Impression Coping OSICP6517N
FDA UDI
Class IActive
Solid Abutment OSSAM4074
FDA UDI
Class IIActive
Angled Abutment OSAA6004NTP
FDA UDI
Class IIActive
Fixture Pin OSFPM
FDA UDI
Class IActive
Pick-Up Impression Coping OSICP4515N
FDA UDI
Class IActive
Bite Impression Coping OBICR6006P
FDA UDI
Class IActive
Fixture POF4007QNP
FDA UDI
Class IIActive
Final Drill OTFD4513
FDA UDI
Class IActive
Cemented Abutment OSCA6075NT
FDA UDI
Class IIActive
Cemented Abutment OSCA6075HT
FDA UDI
Class IIActive
Solid Abutment OSSA4551
FDA UDI
Class IIActive
Cemented Abutment OSCA5052H
FDA UDI
Class IIActive
Cemented Abutment OSCA6044HP
FDA UDI
Class IIActive
Solid Abutment OSSA4072P
FDA UDI
Class IIActive
Solid Abutment OSSA6053T
FDA UDI
Class IIActive
Cemented Abutment OSCA6072N
FDA UDI
Class IIActive
Solid Abutment OSSA4073TP
FDA UDI
Class IIActive
Cemented Abutment OSCA4552HT
FDA UDI
Class IIActive
Bite Impression Coping OBICR4004P
FDA UDI
Class IActive
Healing Abutment OSHA4507G
FDA UDI
Class IIActive
Fixture Driver OFDTC2500
FDA UDI
Class IActive
Bite Impression Coping OBICM4502
FDA UDI
Class IActive
Vertical Anchor NVA2090S
FDA UDI
Class IActive
Bite Scan Body OBICR4503SB
FDA UDI
Class IActive
Fixture Pin OSFPR
FDA UDI
Class IActive
Angled Abutment OSAAM4502NP
FDA UDI
Class IIActive
Solid Abutment OSSAM4042TP
FDA UDI
Class IIActive
Multi Abutment Carrier OMCR1400
FDA UDI
Class IActive
Healing Abutment OSHA5004G
FDA UDI
Class IIActive
Solid Abutment OSSA4073T
FDA UDI
Class IIActive
Final Drill OTFDA5010
FDA UDI
Class IActive

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