Is this your brand? Sign in to claim ownership.

Sign in to claim this brand

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
—
Website
—
LinkedIn
—
Facebook
—
Email
—
Phone
—
PRRC Contact
—
EUDAMED SRN
—
FDA FEI Number
—
DUNS Number
695333960

Catalogue (1771)

Page 3 of 36
DeviceModel / ReferenceRegistriesClassStatus
Angled Abutment OSAA6004AT
FDA UDI
Class IIActive
Healing Abutment OSHAM4503G
FDA UDI
Class IIActive
Fixture Driver NFD21M
FDA UDI
Class IActive
Cemented Abutment OSCA5041NP
FDA UDI
Class IIActive
Solid Abutment OSSAM4551
FDA UDI
Class IIActive
Pick-Up Impression Coping OSICP5011H
FDA UDI
Class IActive
Angled Abutment OSAA6002ATP
FDA UDI
Class IIActive
Impression Coping Driver OBICDLP
FDA UDI
Class IActive
Bite Scan Body OBICR5508SBP
FDA UDI
Class IActive
Pick-Up Impression Coping PIICP6507
FDA UDI
Class IActive
Solid Abutment OSSA4074P
FDA UDI
Class IIActive
Pick-Up Impression Coping OSICP6015NP
FDA UDI
Class IActive
Fixture POF5010QNP
FDA UDI
Class IIActive
Bite Impression Coping OBICR4503P
FDA UDI
Class IActive
Final Drill OTFD7011
FDA UDI
Class IActive
Bite Impression Coping OBICR4003P
FDA UDI
Class IActive
Fixture Driver OFDTC2500EL
FDA UDI
Class IActive
Final Drill OTFDA6507
FDA UDI
Class IActive
Cemented Abutment OSCA4555H
FDA UDI
Class IIActive
Final Drill OTFD4010
FDA UDI
Class IActive
Solid Abutment OSSAM4042T
FDA UDI
Class IIActive
Pick-Up Impression Coping PIICP4807NP
FDA UDI
Class IActive
Cemented Abutment OSCA6073NT
FDA UDI
Class IIActive
Cemented Abutment OSCA6073HT
FDA UDI
Class IIActive
Solid Abutment OSSA6041P
FDA UDI
Class IIActive
Transfer Impression Coping PIICT6512NP
FDA UDI
Class IActive
Mount Extension OMETS
FDA UDI
Class IActive
Pick-Up Impression Coping OSICP6015H
FDA UDI
Class IActive
Cemented Abutment OSCA6075HP
FDA UDI
Class IIActive
Fixture POF6007QNP
FDA UDI
Class IIActive
Transfer Impression Coping OSICT6016HP
FDA UDI
Class IActive
Cemented Abutment OSCA4551N
FDA UDI
Class IIActive
Healing Abutment OSHA7007G
FDA UDI
Class IIActive
Cemented Abutment OSCA6075HTP
FDA UDI
Class IIActive
Transfer Impression Coping OSICT7014N
FDA UDI
Class IActive
Solid Abutment OSSA4571T
FDA UDI
Class IIActive
Angled Abutment OSAAM4502NT
FDA UDI
Class IIActive
Pick-Up Impression Coping OSICPX4511H
FDA UDI
Class IActive
Bite Scan Body OBICM4006SBP
FDA UDI
Class IActive
Bite Scan Body OBICR7008SB
FDA UDI
Class IActive
Solid Abutment OSSA6052T
FDA UDI
Class IIActive
Pick-Up Impression Coping OSICP4517NP
FDA UDI
Class IActive
Cemented Abutment OSCA5043HT
FDA UDI
Class IIActive
Solid Abutment OSSAM4044TP
FDA UDI
Class IIActive
Cap OSSPC605
FDA UDI
Class IIActive
Final Drill NFD3513
FDA UDI
Class IActive
Fixture Driver NFDM25R
FDA UDI
Class IActive
Guide Pin OBICS1608
FDA UDI
Class IActive
Torque Wrench OTW
FDA UDI
Class IActive
Bite Impression Coping OBICR5504P
FDA UDI
Class IActive

Related Companies

Authorised Representatives

No authorised representatives on record.

Importers

Not available yet.

Notified Bodies

Not available yet.

Authorities

Not available yet.