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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 1 of 36
DeviceModel / ReferenceRegistriesClassStatus
Solid Abutment OSSAM4575
FDA UDI
Class IIActive
Cemented Abutment OSCA5042HP
FDA UDI
Class IIActive
Bite Scan Body OBICR5006SB
FDA UDI
Class IActive
Initial Drill NID3010
FDA UDI
Class IActive
Transfer Impression Coping OSICT4514H
FDA UDI
Class IActive
Bite Impression Coping OBICM4003
FDA UDI
Class IActive
Fixture POF6011QNP
FDA UDI
Class IIActive
Final Drill OTFDA5513
FDA UDI
Class IActive
Cemented Abutment OSCA6075NTP
FDA UDI
Class IIActive
Cemented Abutment OSCA7053HP
FDA UDI
Class IIActive
Cemented Abutment OSCA5053HT
FDA UDI
Class IIActive
Healing Abutment OSHAM4003G
FDA UDI
Class IIActive
Fixture Mount Screw OFMIS
FDA UDI
Class IActive
Pick-Up Impression Coping OSICP6017HP
FDA UDI
Class IActive
Final Drill OTFDA6510
FDA UDI
Class IActive
Pick-Up Impression Coping OSICPM4511HP
FDA UDI
Class IActive
Transfer Impression Coping OSICTX4011N
FDA UDI
Class IActive
Initial Drill OID2307
FDA UDI
Class IActive
Cemented Abutment OSCA6044NP
FDA UDI
Class IIActive
Solid Abutment OSSAM4573
FDA UDI
Class IIActive
Solid Abutment OSSA4552P
FDA UDI
Class IIActive
Cemented Abutment OSCA5053NTP
FDA UDI
Class IIActive
Cemented Abutment OSCAM4553HTP
FDA UDI
Class IIActive
Parallel Pin OPP4000
FDA UDI
Class IActive
Torque wrench TW
FDA UDI
Class IActive
Pick-Up Impression Coping OSICPX4517N
FDA UDI
Class IActive
Solid Abutment OSSAM4073P
FDA UDI
Class IIActive
Pick-Up Impression Coping OSICP4011H
FDA UDI
Class IActive
Transfer Impression Coping OSICT5014NP
FDA UDI
Class IActive
Cemented Abutment OSCA5073NTP
FDA UDI
Class IIActive
Bite Impression Coping OBICR7003
FDA UDI
Class IActive
Multi Impression Coping OMICP4808H
FDA UDI
Class IActive
Solid Abutment OSSAM4043
FDA UDI
Class IIActive
Pick-Up Impression Coping OSICPX4015N
FDA UDI
Class IActive
Cemented Abutment OSCA6074N
FDA UDI
Class IIActive
Removal Tool ORTR
FDA UDI
Class IActive
Transfer Impression Coping OSICTX4014NP
FDA UDI
Class IActive
Bite Scan Body OBICR5502SB
FDA UDI
Class IActive
Cemented Abutment OSCA6054H
FDA UDI
Class IIActive
Fixture Tap Drill OFTD5000
FDA UDI
Class IActive
Final Drill OTFDA4508
FDA UDI
Class IActive
Solid Abutment OSSAM4054TP
FDA UDI
Class IIActive
Cemented Abutment OSCA4551NTP
FDA UDI
Class IIActive
Fixture Pin OSFPXS
FDA UDI
Class IActive
Pick-Up Impression Coping PIICP4812
FDA UDI
Class IActive
Transfer Impression Coping OSICTM4011HP
FDA UDI
Class IActive
Cemented Abutment OSCA7051HP
FDA UDI
Class IIActive
Solid Abutment OSSA4542P
FDA UDI
Class IIActive
Healing Abutment OSHAM4507G
FDA UDI
Class IIActive
Fixture Driver OFDM2500EL
FDA UDI
Class IActive

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