Phytron- Elektronik GmbH
GermanyFDA applicant, unverified
- Devices
- 1
What Phytron- Elektronik GmbH makes
Phytron-Elektronik GmbH manufactures the ENDOSTEPPER 1, a motorized drive system designed for precise linear motion control in medical and industrial applications, particularly for orthopedic and surgical instruments requiring accurate positioning.
The ENDOSTEPPER 1 is classified as a Class I medical device in the US and is listed under the FDA’s 510(k) pathway. The company is based in the United States.
Catalogue
Endostepper 1 Ref K993188
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Phytron- Elektronik GmbH have in the registry?
The registry currently lists 1 device for Phytron- Elektronik GmbH. Devices recorded under merged duplicate company entries are counted once.
Which registries list Phytron- Elektronik GmbH's devices?
Among its 1 most recently registered device, Phytron- Elektronik GmbH has devices listed in FDA 510(k) (1 device).
What risk classes do Phytron- Elektronik GmbH's devices fall under?
Among its 1 most recently registered device, the classes recorded for Phytron- Elektronik GmbH's devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Phytron- Elektronik GmbH in the registry?
The most recently registered devices listed for Phytron- Elektronik GmbH include ENDOSTEPPER 1.