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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 19 of 36
DeviceModel / ReferenceRegistriesClassStatus
Temporary Abutment OSTAM4010HP
FDA UDI
Class IIActive
Pick-Up Impression Coping OSICP5015NP
FDA UDI
Class IActive
Cemented Abutment OSCA6073NP
FDA UDI
Class IIActive
Final Drill NFD4011
FDA UDI
Class IActive
Multi Guide Pin OMGP1417
FDA UDI
Class IActive
Transfer Impression Coping OSICT6014HP
FDA UDI
Class IActive
Angled Abutment OSAA6002N
FDA UDI
Class IIActive
Healing Abutment OSHA6004G
FDA UDI
Class IIActive
Transfer Impression Coping PIICT4809N
FDA UDI
Class IActive
Transfer Impression Coping OSICTX4514NP
FDA UDI
Class IActive
Guide Pin OBICS2003
FDA UDI
Class IActive
Bite Scan Body OBICR4008SB
FDA UDI
Class IActive
Angled Abutment OSAA5004NP
FDA UDI
Class IIActive
Pick-Up Impression Coping OSICP5017H
FDA UDI
Class IActive
Solid Abutment OSSA6041
FDA UDI
Class IIActive
Multi Abutment Driver OMDT3300
FDA UDI
Class IActive
Solid Abutment OSSA6073TP
FDA UDI
Class IIActive
Fixture POF4508
FDA UDI
Class IIActive
Solid Abutment OSSA4551T
FDA UDI
Class IIActive
Cemented Abutment OSCA5055HP
FDA UDI
Class IIActive
Transfer Impression Coping OSICTX4511N
FDA UDI
Class IActive
Solid Abutment OSSA6055
FDA UDI
Class IIActive
Cemented Abutment OSCA6042NTP
FDA UDI
Class IIActive
Cemented Abutment OSCA6043HP
FDA UDI
Class IIActive
Scan Body OSBMP
FDA UDI
Class IActive
Cemented Abutment OSCA6053HTP
FDA UDI
Class IIActive
Fixture POF3511Q
FDA UDI
Class IIActive
Solid Abutment OSSAM4554P
FDA UDI
Class IIActive
Solid Driver ORDL4000
FDA UDI
Class IActive
Cemented Abutment OSCA7055N
FDA UDI
Class IIActive
Pick-Up Impression Coping OSICP5515H
FDA UDI
Class IActive
Bite Scan Body OBICR6006SBP
FDA UDI
Class IActive
Solid Abutment OSSA7051T
FDA UDI
Class IIActive
Solid Abutment OSSAM4053T
FDA UDI
Class IIActive
Transfer Impression Coping OSICT4511N
FDA UDI
Class IActive
Fixture POF3513
FDA UDI
Class IIActive
Fixture POF5010
FDA UDI
Class IIActive
Transfer Impression Coping OSICT6016N
FDA UDI
Class IActive
Guide Pin PIGP2010
FDA UDI
Class IActive
Solid Abutment OSSA5054P
FDA UDI
Class IIActive
Pick-Up Impression Coping OSICPM4517HP
FDA UDI
Class IActive
Fixture Pin PSFP3300
FDA UDI
Class IActive
Guide Pin OSICPS
FDA UDI
Class IActive
Plastic Sleeve OSPC4500H
FDA UDI
Class IActive
Healing Abutment OSHA5007G
FDA UDI
Class IIActive
Bone Profile Drill OTBP5500
FDA UDI
Class IActive
Multi Impression Coping OMICT4808N
FDA UDI
Class IActive
Cemented Abutment OSCA5072HP
FDA UDI
Class IIActive
Solid Abutment OSSA4072
FDA UDI
Class IIActive
Bite Impression Coping OBICM4002
FDA UDI
Class IActive

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