Xion GmbH
GermanyFDA applicant, unverified FDA FEI 3003276727
- Devices
- 8
- Registrations
- FDA
- FDA recalls
- 0
At a glance
Market reach
- United States
- FDA FEI
Catalogue
- Registry: GUDID
- Registry: GUDID
- Registry: GUDID
- Registry: GUDID
- Registry: GUDID
- Registry: GUDID
- Registry: GUDID
Nasopharyngoscope, Bronchoscope Ref K070580
Regimes: 510(k) Registry: 510(k)
Company details
- FDA FEI number
- 3003276727
- DUNS number
- 331589812
- Address
- Pankstrasse 8, Berlin
Frequently asked questions
How many devices does Xion GmbH have in the registry?
The registry currently lists 8 devices for Xion GmbH. Devices recorded under merged duplicate company entries are counted once.
Which registries list Xion GmbH's devices?
Among its 8 most recently registered devices, Xion GmbH has devices listed in FDA 510(k) (1 device) and FDA GUDID (7 devices). A device can be listed in more than one registry, so these counts overlap.
What risk classes do Xion GmbH's devices fall under?
Among its 8 most recently registered devices, the classes recorded for Xion GmbH's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Xion GmbH in the registry?
The most recently registered devices listed for Xion GmbH include Arthroscope Ø 2.7 mm, 0°, 140 mm, autoclavable 125 303 100US, Arthroscope Ø 2.7 mm, 30°, 140 mm, autoclavable 125 303 103US, Arthroscope Ø 2.7 mm, 70°, 140 mm, autoclavable 125 303 107US and HD3 Arthroscope Ø 4 mm, 0°, 185 mm, autoclavable 125 304 100UUS.