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Sign in to claim this brandPaltop Advanced Dental Solutions, Ltd.
US
Last updated May 26, 2026
What Paltop Advanced Dental Solutions, Ltd. makes
Paltop Advanced Dental Solutions manufactures dental implant components, including permanent and temporary preformed suprastructures, two-piece screw endosteal implants, and reusable surgical tools like drill bits and screwdrivers. Their portfolio also includes single-use dental implant abutment analogs for intraoral scanning, drilling template guides, and preassembled suprastructure kits designed for dental restoration procedures.
The company’s devices are classified under FDA’s Class I and Class II categories and are listed in the FDA’s Unique Device Identifier (UDI) database. The manufacturer 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 Paltop Advanced Dental Solutions, Ltd. manufacture?
Paltop Advanced Dental Solutions, Ltd. specializes in dental implant components. Their product range includes permanent and temporary preformed suprastructures for dental restorations, two-piece screw endosteal dental implants, reusable surgical tools like drill bits and screwdrivers, single-use dental implant abutment analogs for intraoral scanning, and drilling template guides. These devices are designed to support dental implantation and restoration procedures.
Where is Paltop Advanced Dental Solutions, Ltd. based?
The company is based in the United States. This location is relevant for regulatory compliance and distribution, as it aligns with FDA oversight for medical devices marketed in the US.
Which regulatory registries or databases list Paltop Advanced Dental Solutions, Ltd.’s devices?
Paltop Advanced Dental Solutions, Ltd.’s devices are listed in the FDA’s Unique Device Identifier (UDI) database. This registry ensures traceability and transparency for dental implant components, which are classified under FDA’s Class I and Class II categories.
How are Paltop Advanced Dental Solutions, Ltd.’s devices classified by regulatory authorities?
The company’s devices fall under the FDA’s Class I and Class II classifications. Class I generally includes low-risk devices like reusable surgical tools, while Class II covers moderate-risk items such as dental implants and suprastructures, which require performance standards or special controls to ensure safety and effectiveness.
AI-generated from registry data and not verified by a human reviewer.
Information
- Country
- US
- Address
- —
- Website
- paltopdental.com
- —
- —
- [email protected]
- Phone
- +97246271711
- PRRC Contact
- —
- EUDAMED SRN
- —
- FDA FEI Number
- —
- DUNS Number
- 533836024
Catalogue (1016)
Page 21 of 21| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| Paltop | 60-70103 | FDA UDI | Class I | Active |
| Paltop | 60-70089 | FDA UDI | Class II | Active |
| Paltop | 20-70036P | FDA UDI | Class II | Active |
| Paltop | 30-70110 | FDA UDI | Class I | Active |
| Paltop | 60-70203 | FDA UDI | Class I | Active |
| Paltop | 44-70031 | FDA UDI | Class I | Active |
| Paltop | 30-70508 | FDA UDI | Class I | Active |
| Paltop | 44-72461 | FDA UDI | Class II | Active |
| Paltop | 42-72041 | FDA UDI | Class II | Active |
| Paltop Conical Implant System | K220200 | FDA 510(k) | Class II | Active |
| Paltop Narrow Implant | K210117 | FDA 510(k) | Class II | Active |
| Paltop Dental Implant - Sterile Accessories | K131451 | FDA 510(k) | Class II | Active |
| Paltop Dental Implant System | K112795 | FDA 510(k) | Class II | Active |
| Paltop Narrow Implant, Paltop Short Implant | K130462 | FDA 510(k) | Class II | Active |
| Paltop Short Implants | K232740 | FDA 510(k) | Class II | Active |
| Paltop Dental Implant System | K243983 | FDA 510(k) | Class II | Active |
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FDA Establishments (1)
Establishments registered with the FDA under this company group, matched by name.
- Paltop Advanced Dental Solutions Ltd Caesarea Central · IL FEI 3009161350