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Log10 B.V.

Netherlands NL-MF-000000057 Last updated 17 Sep 2026

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Devices
5
Registries
EUDAMED
FDA recalls
0

Catalogue5

About

Cleaning, disinfecting and sterilizing in an instant Request Demo Always tailored to your workflow Summox's smart all-in-one system guarantees an efficient workflow in dental practice. A streamlined process in which safety and regulation are paramount. Always looking at the team and the patient. More information? Download the brochure via [...]

Translated from the manufacturer's own website. Source

What Log10 B.V. makes

Log10 B.V. manufactures smart containers and sealing systems designed for dental instruments, including full-sized and half-sized containers for general instruments and handpieces, as well as a modular sterilization system called Summox One. These devices integrate automated cleaning, disinfecting, and sterilizing processes to optimize workflow efficiency in dental practices.

The company’s products are classified under EU Medical Device Regulations as Class I and Class IIb, with all devices registered in the EU’s eudamed database. Log10 B.V. is based in the Netherlands.

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 Log10 B.V. manufacture?

Log10 B.V. specializes in smart containers and sealing systems tailored for dental instruments. Their portfolio includes full-sized and half-sized containers for general instruments and handpieces, as well as the Summox One System—a modular sterilization solution. These devices are designed to automate cleaning, disinfecting, and sterilizing processes, improving efficiency in dental workflows.

Where is Log10 B.V. based?

Log10 B.V. is headquartered in the Netherlands, where it develops and manufactures its dental instrument processing solutions.

Which regulatory registries list Log10 B.V.’s devices?

All of Log10 B.V.’s devices are registered in the eudamed database, the official EU registry for medical devices under the Medical Device Regulations (MDR). This ensures transparency and compliance with EU requirements.

How are Log10 B.V.’s devices classified under EU regulations?

Log10 B.V.’s devices fall under Class I and Class IIb classifications under the EU Medical Device Regulations. The classification depends on factors like the device’s intended use, risk level, and interaction with patients (e.g., sterilization systems for reusable instruments carry higher risk and are classified as Class IIb).

Why do some of Log10 B.V.’s devices require a Class IIb classification?

The Class IIb designation for certain devices—like automated sterilization systems—reflects their higher risk profile. These systems directly impact patient safety by ensuring instruments are sterilized before reuse, requiring stricter regulatory oversight to mitigate risks like contamination or improper sterilization cycles.

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

Information

Country
Netherlands
Address
85, Quinten Matsyslaan, Eindhoven, Netherlands
PRRC contact
Jolande Bakker
EUDAMED SRN
NL-MF-000000057