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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 8 of 36
DeviceModel / ReferenceRegistriesClassStatus
Solid Abutment OSSAM4544T
FDA UDI
Class IIActive
Final Drill OTFDA6011
FDA UDI
Class IActive
Fixture Mount OFMR
FDA UDI
Class IActive
Solid Abutment OSSA6042P
FDA UDI
Class IIActive
Cemented Abutment OSCAM4554HTP
FDA UDI
Class IIActive
Angled Abutment OSAA6002AP
FDA UDI
Class IIActive
Cemented Abutment OSCAM4553HP
FDA UDI
Class IIActive
Solid Abutment OSSA4544
FDA UDI
Class IIActive
Solid Abutment OSSA4552
FDA UDI
Class IIActive
Cemented Abutment OSCA6044NT
FDA UDI
Class IIActive
Transfer Impression Coping OSICT4016N
FDA UDI
Class IActive
Bite Scan Body OBICR4003SB
FDA UDI
Class IActive
Solid Abutment OSSAM4555T
FDA UDI
Class IIActive
Solid Abutment OSSA6054
FDA UDI
Class IIActive
Pick-Up Impression Coping OSICP5015H
FDA UDI
Class IActive
Bite Scan Body OBICR5504SBP
FDA UDI
Class IActive
Cemented Abutment OSCA4554HTP
FDA UDI
Class IIActive
Transfer Impression Coping PIICT4809P
FDA UDI
Class IActive
Bite Scan Body OBICR5508SB
FDA UDI
Class IActive
Slot Driver OMDEL0600
FDA UDI
Class IActive
Solid Abutment OSSAM4054P
FDA UDI
Class IIActive
Fixture Driver OFDM2100EL
FDA UDI
Class IActive
Final Drill OTFD4510
FDA UDI
Class IActive
Pick-Up Impression Coping PIICP6512P
FDA UDI
Class IActive
Fixture POF4510Q
FDA UDI
Class IIActive
Transfer Impression Coping OSICT4011HP
FDA UDI
Class IActive
Transfer Impression Coping OSICT5016N
FDA UDI
Class IActive
Transfer Impression Coping OSICTX4514H
FDA UDI
Class IActive
Cemented Abutment OSCA4552NTP
FDA UDI
Class IIActive
Cemented Abutment OSCA6042H
FDA UDI
Class IIActive
Solid Abutment OSSA5053
FDA UDI
Class IIActive
Bite Impression Coping OBICR7002
FDA UDI
Class IActive
Fixture POF5011Q
FDA UDI
Class IIActive
Cemented Abutment OSCA6041HTP
FDA UDI
Class IIActive
Temporary Abutment OSTAM4030NP
FDA UDI
Class IIActive
Cemented Abutment OSCA5041HP
FDA UDI
Class IIActive
Bite Scan Body OBICR4006SBP
FDA UDI
Class IActive
Hex Driver PHD1300
FDA UDI
Class IActive
Cemented Abutment OSCAM4555NP
FDA UDI
Class IIActive
Transfer Impression Coping OSICTX4011NP
FDA UDI
Class IActive
Fixture Tap Drill OFTD4500
FDA UDI
Class IActive
Cemented Abutment OSCA7051N
FDA UDI
Class IIActive
Cemented Abutment OSCA5052HTP
FDA UDI
Class IIActive
Pick-Up Impression Coping OSICPX4515H
FDA UDI
Class IActive
Pick-Up Impression Coping OSICP4011N
FDA UDI
Class IActive
Fixture POF4010Q
FDA UDI
Class IIActive
Cemented Abutment OSCA5045NTP
FDA UDI
Class IIActive
Bite Scan Body OBICM4002SB
FDA UDI
Class IActive
Pick-Up Impression Coping OSICPX4015NP
FDA UDI
Class IActive
Fixture Mount OFMM
FDA UDI
Class IActive

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