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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)

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DeviceModel / ReferenceRegistriesClassStatus
Angled Abutment OSAA5004BP
FDA UDI
Class IIActive
Pick-up Impression Coping OSICP5517H
FDA UDI
Class IActive
Solid Abutment OSSA5073TP
FDA UDI
Class IIActive
Fixture Pin OSFPMS
FDA UDI
Class IActive
Cemented Abutment OSCA6073HP
FDA UDI
Class IIActive
Fixture Driver OFDT3100L
FDA UDI
Class IActive
Pick-Up Impression Coping OSICPX4515N
FDA UDI
Class IActive
Healing Abutment OSHA4503G
FDA UDI
Class IIActive
Solid Abutment OSSA4553T
FDA UDI
Class IIActive
Solid Abutment OSSA4052
FDA UDI
Class IIActive
Solid Abutment OSSAM4055T
FDA UDI
Class IIActive
Cemented Abutment OSCA5045NP
FDA UDI
Class IIActive
Cemented Abutment OSCA4555NT
FDA UDI
Class IIActive
Cap OSSPC454
FDA UDI
Class IIActive
Solid Abutment OSSA6073T
FDA UDI
Class IIActive
Digital Lab Analog ODLA350
FDA UDI
Class IActive
Fixture POF4013
FDA UDI
Class IIActive
Temporary Abutment OSTA4530N
FDA UDI
Class IIActive
Angled Abutment OSAAM4502BP
FDA UDI
Class IIActive
Cemented Abutment OSCAM4551N
FDA UDI
Class IIActive
Hex Driver OTDS1207
FDA UDI
Class IActive
Solid Abutment OSSA5054T
FDA UDI
Class IIActive
Angled Abutment OSAA5004ATP
FDA UDI
Class IIActive
Solid Abutment OSSAM4071T
FDA UDI
Class IIActive
Solid Abutment OSSA4051P
FDA UDI
Class IIActive
Cemented Abutment OSCA5072HT
FDA UDI
Class IIActive
Pick-Up Impression Coping OSICP6511NP
FDA UDI
Class IActive
Cemented Abutment OSCA7052H
FDA UDI
Class IIActive
Guide Pin OBICS2004
FDA UDI
Class IActive
Cemented Abutment OSCA6054NTP
FDA UDI
Class IIActive
Pick-Up Impression Coping OSICPM4011H
FDA UDI
Class IActive
Final Drill OTFDA7010
FDA UDI
Class IActive
Cemented Abutment OSCA4555NTP
FDA UDI
Class IIActive
Cap OSSPC407
FDA UDI
Class IIActive
Final Drill NFD5013
FDA UDI
Class IActive
Cemented Abutment OSCA4553NTP
FDA UDI
Class IIActive
Fixture Driver OFDT3100EL
FDA UDI
Class IActive
Cemented Abutment OSCA5053H
FDA UDI
Class IIActive
Cemented Abutment OSCA7054HP
FDA UDI
Class IIActive
Fixture POF5011QNP
FDA UDI
Class IIActive
Plastic Sleeve OIPC4800H
FDA UDI
Class IActive
Solid Abutment OSSA4073
FDA UDI
Class IIActive
Cemented Abutment OSCAM4555NT
FDA UDI
Class IIActive
Solid Abutment OSSAM4055
FDA UDI
Class IIActive
Fixture POF3510QNP
FDA UDI
Class IIActive
Cemented Abutment OSCA5073HP
FDA UDI
Class IIActive
Final Drill OTFDA6010
FDA UDI
Class IActive
Transfer Impression Coping OSICT7016H
FDA UDI
Class IActive
Pick-Up Impression Coping OSICP5017HP
FDA UDI
Class IActive
Solid Abutment OSSA4572
FDA UDI
Class IIActive

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