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Sign in to claim this brandQuickdent Devices Private , Ltd.
US
Last updated May 23, 2026
What Quickdent Devices Private , Ltd. makes
Quickdent Devices Private, Ltd. manufactures dental implant systems, including straight and conical abutments, internal hex platforms, and housing inserts for implant-supported restorations. Their portfolio includes components like the IH Straight Abutment, Korticale TPR IH, Trabecos IH Internal Hex, and Actifix CC Conical Narrow Platform, designed for osseointegrated dental implants.
The company’s devices are classified as Class II under FDA regulations and are listed via 510(k) and UDI pathways. Their products are registered in the US, where the manufacturer is based.
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 Quickdent Devices Private, Ltd. manufacture?
Quickdent Devices Private, Ltd. specializes in dental implant systems, focusing on components like abutments and housing inserts. Their portfolio includes straight and conical abutments, internal hex platforms, and other fixtures used in implant-supported restorations, such as the IH Straight Abutment, Korticale TPR IH, and Actifix CC Conical Narrow Platform. These devices are designed to support osseointegrated dental implants, ensuring stability and compatibility with restorative procedures.
Where is Quickdent Devices Private, Ltd. based, and where are their devices used?
Quickdent Devices Private, Ltd. is based in the United States. Their devices are registered and intended for use in the US market, where they are subject to regulatory oversight by the FDA. The company’s focus on dental implant systems aligns with the US healthcare landscape, particularly in restorative dentistry.
Which regulatory registries list Quickdent Devices Private, Ltd.’s devices?
Quickdent Devices Private, Ltd.’s devices are listed in the FDA’s 510(k) premarket notification pathway and the Unique Device Identifier (UDI) system. These registries ensure traceability and compliance with US regulatory requirements for Class II medical devices, which includes dental implant components.
How are Quickdent Devices Private, Ltd.’s devices classified under FDA regulations?
Quickdent Devices Private, Ltd.’s dental implant systems fall under FDA Class II classification. This classification is typically assigned to devices that pose moderate risk and require special controls beyond general controls to ensure safety and effectiveness, such as dental implants that require validation of biocompatibility and performance standards.
AI-generated from registry data and not verified by a human reviewer.
Information
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- US
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Catalogue (119)
Page 3 of 3| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| Ossi Classic IH | 3.75 x 11.5mm | FDA UDI | Class II | Active |
| Trabecos IH Internal Hex | 3.5 x 11.5mm | FDA UDI | Class II | Active |
| Quickloc and Quicksnap CC Housing Insert | Pink | FDA UDI | Class II | Active |
| Ossi Classic IH | 4.2 x 11.5mm | FDA UDI | Class II | Active |
| Ossi Classic IH | 4.2 x 13mm | FDA UDI | Class II | Active |
| IH Straight Abutment | 5mm | FDA UDI | Class II | Active |
| IH Straight Abutment Wide | 13mm | FDA UDI | Class II | Active |
| Trabecos IH Internal Hex | 4.2 x 8mm | FDA UDI | Class II | Active |
| Kortifix Pro CC | 4.2 x 12mm | FDA UDI | Class II | Active |
| Trabecos IH Internal Hex | 3.5 x 13mm | FDA UDI | Class II | Active |
| Ossi Classic IH | 4.2 x 16mm | FDA UDI | Class II | Active |
| Actifix CC Conical Narrow Platform | 4.2 x 13mm | FDA UDI | Class II | Active |
| Korticale TPR IH | 3.5 x 10mm | FDA UDI | Class II | Active |
| IH Straight Abutment Wide | 9mm | FDA UDI | Class II | Active |
| Ossi Classic IH | 3.5 x 10mm | FDA UDI | Class II | Active |
| Ossi Classic IH | 6.0 x 11.5mm | FDA UDI | Class II | Active |
| IH Straight Abutment Narrow | 7mm | FDA UDI | Class II | Active |
| Korticale SP | 3.5 x 16mm | FDA UDI | Class II | Active |
| Quickdent Dental Implant System | K243094 | 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.
- Quickdent Devices Private Limited Mumbai Maharashtra · IN FEI 3036779616