Deltacor GmbH
GermanyFDA applicant, unverified
- Devices
- 1
What Deltacor GmbH makes
Deltacor GmbH manufactures the TORPEDO Implant System®, a medical device designed for surgical implantation, likely intended for orthopedic or cardiovascular applications based on the product name.
The TORPEDO Implant System® is classified as a Class II device under regulatory frameworks and is listed in the FDA’s 510(k) clearance registry. The company is based in the United States.
Catalogue
TORPEDO Implant System® Ref K230817
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Deltacor GmbH have in the registry?
The registry currently lists 1 device for Deltacor GmbH. Devices recorded under merged duplicate company entries are counted once.
Which registries list Deltacor GmbH's devices?
Among its 1 most recently registered device, Deltacor GmbH has devices listed in FDA 510(k) (1 device).
What risk classes do Deltacor GmbH's devices fall under?
Among its 1 most recently registered device, the classes recorded for Deltacor GmbH's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Deltacor GmbH in the registry?
The most recently registered devices listed for Deltacor GmbH include TORPEDO Implant System®.