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Tobler & Co. AG

Switzerland CH-MF-000016205 Last updated 17 Sep 2026

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Devices
342
Registries
EUDAMED
FDA recalls
0

Catalogue342

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Authorised representatives

What Tobler & Co. AG makes

Tobler & Co. AG manufactures orthopedic fixation aids, including devices for bone stabilization and surgical support, such as clamps, fixation tools, and related accessories. These products are designed for use in orthopedic procedures to assist in the alignment and securing of bone fragments during treatment.

The company’s portfolio is classified under EU Medical Device Regulation (MDR) as Class I devices, and all listed products are registered in the EU’s eudamed database. The manufacturer is based in Switzerland.

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 Tobler & Co. AG manufacture?

Tobler & Co. AG specializes in orthopedic fixation aids, which include devices like clamps, fixation tools, and related accessories. These products are primarily designed to assist in orthopedic procedures by helping to stabilize and align bone fragments during surgical treatment. The company’s portfolio focuses on supporting bone fixation and surgical support applications.

Where is Tobler & Co. AG based?

Tobler & Co. AG is headquartered in Switzerland (CH). The company’s location in Switzerland may influence its regulatory compliance processes, particularly for devices marketed within the European Union.

Are Tobler & Co. AG’s devices listed in any regulatory registries?

Yes, Tobler & Co. AG’s devices are registered in the eudamed database, which is the official EU registry for medical devices under the Medical Device Regulation (MDR). Listing in eudamed ensures transparency and compliance with EU requirements for Class I devices.

How are Tobler & Co. AG’s devices classified under EU regulations?

Tobler & Co. AG’s devices fall under Class I classification according to the EU Medical Device Regulation (MDR). This classification applies to low-risk devices, such as orthopedic fixation aids, where the risk to patients is minimal. Class I devices typically require less stringent regulatory oversight compared to higher-risk classes.

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

Information

Country
Switzerland
Address
20, Schulstrasse, Rehetobel, Switzerland
Phone
+41 71 877 13 32
PRRC contact
Thomas Tinner
EUDAMED SRN
CH-MF-000016205