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SURGICON AG

Switzerland CH-MF-000020566 Last updated 23 Oct 2026

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Devices
258
Registries
EUDAMEDFDA
FDA recalls
0

Catalogue258

Page 1 of 6

Showing 1-50 of 258

What SURGICON AG makes

Surgicon AG manufactures surgical knives and blades for ophthalmic procedures, including slit-angle and clear-cornea variants, as well as microvascular reconstruction (MVR) tools in 20G, 21G, and 23G sizes. Some products feature protective guards, angled or straight designs, and single-bevel cutting edges. The portfolio also includes angled and straight blades for specific surgical applications.

The company’s devices are classified as Class IIa under EU regulations and are registered in the EUDAMED database. Surgicon AG 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 Surgicon AG manufacture?

Surgicon AG specializes in surgical knives and blades designed specifically for ophthalmic (eye) procedures. Their portfolio includes slit-angle and clear-cornea blades, as well as microvascular reconstruction (MVR) tools in various gauges (20G, 21G, and 23G). Some products feature protective guards, angled or straight designs, and single-bevel cutting edges to suit different surgical needs.

Where is Surgicon AG based?

Surgicon AG is headquartered in Switzerland, as indicated by the country code 'CH' associated with the company. This location is relevant for regulatory compliance and distribution within the European market.

Which regulatory registries list Surgicon AG’s devices?

Surgicon AG’s devices are registered in the EUDAMED database, which is the official European Union database for medical devices. This registry is used to track and verify the compliance of devices marketed within the EU, ensuring transparency and traceability.

How are Surgicon AG’s devices classified under EU regulations?

Surgicon AG’s devices fall under Class IIa classification according to EU medical device regulations. This classification applies to devices that pose a low to moderate risk, requiring specific conformity assessment procedures to ensure safety and performance before they can be placed on the market.

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

Information

Country
Switzerland
Address
3, Lerchenfeldstrasse, St.Gallen, Switzerland
Website
surgicon.ch
PRRC contact
Manisha Ishwar Poojary
EUDAMED SRN
CH-MF-000020566
FDA FEI number
3022137228