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Sign in to claim this brandSIC invent AG
US
Last updated May 24, 2026
What SIC invent AG makes
The company produces dental implant components, including permanent and temporary preformed suprastructures, two-piece screw endosteal implants, reusable dental drill bits, and precision attachments for implant bars. It also supplies reusable holding endpieces, implant extractors, and dental implant analogs for laboratory use.
These 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 SIC invent AG manufacture?
SIC invent AG specializes in dental implant components. Their product range includes permanent and temporary preformed suprastructures for dental implants, two-piece screw endosteal dental implants, reusable dental drill bits, bar dental precision attachments, reusable holding endpieces, implant extractors, and dental implant analogs used in laboratory settings. These devices support various stages of dental implant procedures, from initial placement to final restoration.
Where is SIC invent AG based, and what does that mean for their regulatory compliance?
SIC invent AG is based in the United States. Since the company’s devices are listed in the FDA’s Unique Device Identifier (UDI) database, this indicates their products are intended for the US market and must comply with FDA regulations. The FDA classifies their devices as either Class I or Class II, which determines the level of regulatory oversight and requirements for premarket submission.
Which regulatory registries or databases list SIC invent AG’s devices?
SIC invent AG’s devices are included 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 specific to the US market and reflects compliance with FDA requirements for device identification.
How are SIC invent AG’s dental implant devices classified under FDA regulations?
SIC invent AG’s devices fall under two FDA classification categories: Class I and Class II. Class I devices generally pose minimal risk and may require general controls, while Class II devices involve a higher level of risk and require special controls to ensure safety and effectiveness. The classification determines the regulatory pathway, such as whether a 510(k) premarket notification submission is required for Class II devices, whereas Class I devices may only need registration and listing.
What does it mean for SIC invent AG’s devices to be listed in the FDA’s UDI database?
Listing in the FDA’s UDI database means that each of SIC invent AG’s devices has been assigned a unique identifier, combining a device identifier and a production identifier. This system improves patient safety, enhances regulatory oversight, and facilitates better tracking of devices in the supply chain. It also helps healthcare providers and regulators quickly access critical information about the device, such as its manufacturer, model, and batch details, ensuring compliance with FDA requirements for medical device traceability.
AI-generated from registry data and not verified by a human reviewer.
Information
- Country
- US
- Address
- —
- Website
- sic-invent.com
- —
- —
- [email protected]
- Phone
- +41612602460
- PRRC Contact
- —
- EUDAMED SRN
- —
- FDA FEI Number
- —
- DUNS Number
- 482083990
Catalogue (589)
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FDA Establishments (1)
Establishments registered with the FDA under this company group, matched by name.
- Sic Invent Ag Basel Town Basel-Landschaft · CH FEI 3004443656