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Sign in to claim this brandImplant 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
- —
- Website
- implantlogistics.com
- —
- —
- [email protected]
- Phone
- 1-844-383-8001
- PRRC Contact
- —
- EUDAMED SRN
- —
- FDA FEI Number
- —
- DUNS Number
- 079280537
Catalogue (724)
Page 15 of 15| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| Implant-One | IT2520 | FDA UDI | Class I | Active |
| Implant-One | ALR-0350-00 | FDA UDI | Class II | Active |
| Implant-One | AS-160 | FDA UDI | Class II | Active |
| Implant-One | ATB-0415-00 | FDA UDI | Class II | Active |
| Implant-One | PLP-2030-00 | FDA UDI | Class I | Active |
| Implant-One | 1123-3305-00 | FDA UDI | Class II | Active |
| Implant-One | ABL-0420-00 | FDA UDI | Class II | Active |
| Implant-One | SD32022 | FDA UDI | Class I | Active |
| Implant-One | ABL-0430-00 | FDA UDI | Class II | Active |
| Implant-One | HCN-0410-00 | FDA UDI | Class II | Active |
| Implant-One | ACM-0115-AR | FDA UDI | Class II | Active |
| Implant-One | MUA-0335-17M | FDA UDI | Class II | Active |
| Implant-One | RAM-MARK-20 | FDA UDI | Class I | Active |
| Implant-One | IT230-00 | FDA UDI | Class II | Active |
| Implant-One | CSR-0400-00 | FDA UDI | Class II | Active |
| Implant-One | SDL37522 | FDA UDI | Class I | Active |
| Implant-One | HHS-0400-00 | FDA UDI | Class II | Active |
| Implant-One | IW5-6510-00 | FDA UDI | Class II | Unknown |
| Implant-One | IT221-50 | FDA UDI | Class II | Active |
| Implant-One | ABL-0530-00 | FDA UDI | Class II | Active |
| Implant-One | IT221-20 | FDA UDI | Class II | Active |
| Implant-One | IT140-20 | FDA UDI | Class II | Active |
| Implant-One | MUA-0425-17M | FDA UDI | Class II | Active |
| Implant-One Multi-Unit Abutment | K212394 | FDA 510(k) | Class II | Active |
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