Antyllos Medizintechnik GmbH
GermanyFDA applicant, unverified
- Devices
- 1
What Antyllos Medizintechnik GmbH makes
Antyllos Medizintechnik GmbH manufactures endoscopic tube shaft instruments designed for monopolar coagulation, used in minimally invasive surgical procedures to seal or cut tissue with electrical current.
These devices are classified as Class II under FDA regulations and are listed via the 510(k) pathway. The company is based in the United States.
Catalogue
- Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Antyllos Medizintechnik GmbH have in the registry?
The registry currently lists 1 device for Antyllos Medizintechnik GmbH. Devices recorded under merged duplicate company entries are counted once.
Which registries list Antyllos Medizintechnik GmbH's devices?
Among its 1 most recently registered device, Antyllos Medizintechnik GmbH has devices listed in FDA 510(k) (1 device).
What risk classes do Antyllos Medizintechnik GmbH's devices fall under?
Among its 1 most recently registered device, the classes recorded for Antyllos Medizintechnik GmbH's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Antyllos Medizintechnik GmbH in the registry?
The most recently registered devices listed for Antyllos Medizintechnik GmbH include ENDOSCOPIC TUBE SHAFT INSTRUMENTS FOR MONOPLAR COAGULATION.