Heager GmbH
GermanyFDA applicant, unverified FDA FEI 3015976667
- Devices
- 1
- Registrations
- FDA
- FDA recalls
- 0
At a glance
Market reach
- United States
- FDA FEI
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
Heager Medical Laser Family (Sabrina/Adolf) Ref K250261
Regimes: 510(k) Registry: 510(k)
Company details
- FDA FEI number
- 3015976667
- Address
- Friedrich Elbert Strabe, HAAN North Rhine-Westphalia
Frequently asked questions
How many devices does Heager GmbH have in the registry?
The registry currently lists 1 device for Heager GmbH. Devices recorded under merged duplicate company entries are counted once.
Which registries list Heager GmbH's devices?
Among its 1 most recently registered device, Heager GmbH has devices listed in FDA 510(k) (1 device).
What risk classes do Heager GmbH's devices fall under?
Among its 1 most recently registered device, the classes recorded for Heager GmbH's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Heager GmbH in the registry?
The most recently registered devices listed for Heager GmbH include Heager Medical Laser Family (Sabrina/Adolf).