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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 2 of 36
DeviceModel / ReferenceRegistriesClassStatus
Solid Abutment OSSA5043T
FDA UDI
Class IIActive
Final Drill OTFD7013N
FDA UDI
Class IActive
Transfer Impression Coping OSICTM4511N
FDA UDI
Class IActive
Pick-Up Impression Coping OSICPX4017HP
FDA UDI
Class IActive
Hex Driver OTDL1200
FDA UDI
Class IActive
Solid Abutment OSSAM4074T
FDA UDI
Class IIActive
Pick-Up Impression Coping OSICPM4517H
FDA UDI
Class IActive
Bite Impression Coping OBICR5006
FDA UDI
Class IActive
Cemented Abutment OSCA7051HTP
FDA UDI
Class IIActive
Fixture POF7007
FDA UDI
Class IIActive
Multi Guide Pin OMGP1420
FDA UDI
Class IActive
Final Drill OTFDA7013
FDA UDI
Class IActive
Cemented Abutment OSCA6053N
FDA UDI
Class IIActive
Cemented Abutment OSCA6054NP
FDA UDI
Class IIActive
Hex Driver OTSDS1200
FDA UDI
Class IActive
Transfer Impression Coping OSICT4514NP
FDA UDI
Class IActive
Fixture Tap Drill OFTD4000
FDA UDI
Class IActive
Solid Abutment OSSAM4053
FDA UDI
Class IIActive
Cemented Abutment OSCA5045HP
FDA UDI
Class IIActive
Solid Abutment OSSA7054
FDA UDI
Class IIActive
Transfer Impression Coping OSICT5516N
FDA UDI
Class IActive
Bite Impression Coping OBICR4508P
FDA UDI
Class IActive
Solid Abutment OSSAM4572T
FDA UDI
Class IIActive
Scan Body ISBW
FDA UDI
Class IActive
Initial Drill NID2211
FDA UDI
Class IActive
Bite Impression Coping OBICM4006P
FDA UDI
Class IActive
Transfer Impression Coping OSICTM4014HP
FDA UDI
Class IActive
Osteotome OST28
FDA UDI
Class IActive
Transfer Impression Coping OSICTM4514HP
FDA UDI
Class IActive
Transfer Impression Coping OSICT6011NP
FDA UDI
Class IActive
Solid Abutment OSSA5045
FDA UDI
Class IIActive
Solid Abutment OSSAM4541T
FDA UDI
Class IIActive
Solid Abutment OSSAM4043TP
FDA UDI
Class IIActive
Final Drill OTFDA4007
FDA UDI
Class IActive
Solid Abutment OSSA4552TP
FDA UDI
Class IIActive
Solid Abutment OSSA4045P
FDA UDI
Class IIActive
Cemented Abutment OSCA4553HT
FDA UDI
Class IIActive
Cemented Abutment OSCA6045HT
FDA UDI
Class IIActive
Cemented Abutment OSCAM4552H
FDA UDI
Class IIActive
Cortical Drill OTCD6500
FDA UDI
Class IActive
Transfer Impression Coping OSICT5514NP
FDA UDI
Class IActive
Solid Abutment OSSA4042
FDA UDI
Class IIActive
Temporary Abutment OSTA4510N
FDA UDI
Class IIActive
Hex Driver OTDS1215
FDA UDI
Class IActive
Guide Pin OBICS1602
FDA UDI
Class IActive
Cemented Abutment OSCA6043HTP
FDA UDI
Class IIActive
Solid Abutment OSSA6074TP
FDA UDI
Class IIActive
Cap OSSPC504
FDA UDI
Class IIActive
Cemented Abutment OSCA5045HTP
FDA UDI
Class IIActive
Angled Abutment OSAA5002BP
FDA UDI
Class IIActive

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