Sodexco
Country not established
- Devices
- 1
What Sodexco makes
Sodexco manufactures the Princess Syringe, a single-use, pre-filled syringe designed for precise medication delivery in clinical settings.
The Princess Syringe is classified as a Class I medical device under FDA regulations and is listed via the 510(k) pathway. The company is based in the United States.
Catalogue
Princess Syringe Ref K980577
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Sodexco have in the registry?
The registry currently lists 1 device for Sodexco. Devices recorded under merged duplicate company entries are counted once.
Which registries list Sodexco's devices?
Among its 1 most recently registered device, Sodexco has devices listed in FDA 510(k) (1 device).
What risk classes do Sodexco's devices fall under?
Among its 1 most recently registered device, the classes recorded for Sodexco's devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Sodexco in the registry?
The most recently registered devices listed for Sodexco include PRINCESS SYRINGE.