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Implant Logistics, Inc.

US

Last updated May 26, 2026

What Implant Logistics, Inc. makes

Implant Logistics, Inc. manufactures dental implant suprastructures, including permanent and temporary preformed types, as well as single-use temporary variants. Their portfolio also includes reusable dental drill bits, two-piece endosteal dental implants, and reusable surgical screwdrivers. Additional products encompass dental prosthesis/implant abutment screws, intraoral-scanning abutment analogs (single-use), and comprehensive dental implant systems.

The company’s devices are regulated under FDA’s Class I and Class II classifications and are listed in the FDA’s Unique Device Identifier (UDI) database. Implant Logistics, Inc. is based in the United States.

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 Implant Logistics, Inc. manufacture?

Implant Logistics, Inc. specializes in dental implant-related devices. Their portfolio includes permanent and temporary preformed dental implant suprastructures, single-use temporary suprastructures, reusable dental drill bits, two-piece endosteal dental implants, reusable surgical screwdrivers, dental prosthesis/implant abutment screws, single-use intraoral-scanning abutment analogs, and full dental implant systems. These products focus on components used in dental restoration and implantology.

Where is Implant Logistics, Inc. based, and how does that affect its devices?

Implant Logistics, Inc. is based in the United States. Since the company operates within the U.S., its devices are subject to FDA regulations, including classification under FDA’s Class I and Class II categories. This means their products must comply with FDA requirements for safety, performance, and labeling, ensuring they meet U.S. standards for medical devices.

Which regulatory registries or databases list Implant Logistics, Inc.’s devices?

Implant Logistics, Inc.’s devices are listed in the FDA’s Unique Device Identifier (UDI) database. The UDI system helps track and identify medical devices throughout their distribution and use, ensuring transparency and traceability for regulatory and clinical purposes. This listing is essential for compliance and identification in the U.S. market.

How are Implant Logistics, Inc.’s devices classified under FDA regulations?

Implant Logistics, Inc.’s devices fall under FDA’s Class I and Class II classifications. Class I devices generally pose minimal risk and may require general controls, while Class II devices involve a higher risk and require special controls to ensure safety and effectiveness. The classification depends on factors like the device’s purpose, potential risks, and intended use in dental implantology.

What does it mean for Implant Logistics, Inc.’s devices to be listed in the FDA’s UDI database?

Listing in the FDA’s UDI database means each of Implant Logistics, Inc.’s devices has a unique identifier assigned to it, combining a device identifier and a production identifier. This system improves device tracking, reduces medical errors, and supports regulatory oversight by ensuring accurate identification and traceability of products throughout their lifecycle. It’s a requirement for compliance in the U.S. market.

AI-generated from registry data and not verified by a human reviewer.

Information

Country
US
Address
—
LinkedIn
—
Facebook
—
Phone
1-844-383-8001
PRRC Contact
—
EUDAMED SRN
—
FDA FEI Number
—
DUNS Number
079280537

Catalogue (724)

Page 11 of 15
DeviceModel / ReferenceRegistriesClassStatus
Implant-One DEN-0345-SB
FDA UDI
Class IActive
Implant-One HCS-0510-00
FDA UDI
Class IIActive
Implant-One IT200-4014
FDA UDI
Class IIActive
Implant-One IW3-4114-CL
FDA UDI
Class IIActive
Implant-One IOS-0400-00
FDA UDI
Class IActive
Implant-One IT200-42510
FDA UDI
Class IIActive
Implant-One IPC-1
FDA UDI
Class IActive
Implant-One AWP-0410-00
FDA UDI
Class IIActive
Implant-One ST519
FDA UDI
Class IActive
Implant-One ATB-0505-00
FDA UDI
Class IIActive
Implant-One 1123-4803-00
FDA UDI
Class IIActive
Implant-One ALR-0340-00
FDA UDI
Class IIActive
Implant-One IT137-SCAN
FDA UDI
Class IActive
Implant-One ALR-0470-00
FDA UDI
Class IIActive
Implant-One IT200-5510
FDA UDI
Class IIActive
Implant-One DEN-0325-30
FDA UDI
Class IIActive
Implant-One IT235-70
FDA UDI
Class IIActive
Implant-One AS-460
FDA UDI
Class IIActive
Implant-One APT-0350-00
FDA UDI
Class IIActive
Implant-One IT120-50
FDA UDI
Class IIActive
Implant-One APT-0405-00
FDA UDI
Class IIActive
Implant-One IT238-50
FDA UDI
Class IIActive
Implant-One IT243-30
FDA UDI
Class IIActive
Implant-One IT235-20
FDA UDI
Class IIActive
Implant-One DGS-1520-FP
FDA UDI
Class IActive
Implant-One AS-310
FDA UDI
Class IIActive
Implant-One RAM-SCRW-06
FDA UDI
Class IIActive
Implant-One AWP-0550-00
FDA UDI
Class IIActive
Implant-One APT-0430-15
FDA UDI
Class IIActive
Implant-One IT240-40
FDA UDI
Class IIActive
Implant-One IT143-20
FDA UDI
Class IIActive
Implant-One ALR-0405-00
FDA UDI
Class IIActive
Implant-One IR5-5514-00
FDA UDI
Class IIUnknown
Implant-One RAM-SCRW-12
FDA UDI
Class IIActive
Implant-One IT121-30
FDA UDI
Class IIActive
Implant-One ALG-0500-09
FDA UDI
Class IActive
Implant-One IT125-20
FDA UDI
Class IIActive
Implant-One IR4-4514-CL
FDA UDI
Class IIActive
Implant-One APT-0320-00
FDA UDI
Class IIActive
Implant-One ASL-0340-00
FDA UDI
Class IIActive
Implant-One IT16412
FDA UDI
Class IActive
Implant-One APT-0550-30
FDA UDI
Class IIActive
Implant-One ATM-0430-00
FDA UDI
Class IIActive
Implant-One DRS-2017-01
FDA UDI
Class IActive
Implant-One ALR-0510-00
FDA UDI
Class IIActive
Implant-One IT100-32514
FDA UDI
Class IIActive
Implant-One MUA-0450-00
FDA UDI
Class IIActive
Implant-One MUA-0520-00
FDA UDI
Class IIActive
Implant-One KIT-RAMS-00
FDA UDI
Class IActive
Implant-One IT133-20
FDA UDI
Class IIActive

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