FDA Device Entity Profile: Xenios AG

Known Identifiers & Locations

FEI Numbers 3002845651, 3012172416, 3030191221

Owner Operator Numbers 10045964

Locations Covered Heilbronn Baden-Wurttemberg, DE; Reutlingen Baden-Wurttemberg, DE; Stolberg North Rhine-Westphalia, DE

Registered Establishments (3)

Registration #	Establishment Name	Location	Establishment Type(s)	Action
3002845651	XENIOS AG	Stolberg North Rhine-Westphalia, DE	Manufacture Medical Device	View Details
3012172416	Xenios AG	Heilbronn Baden-Wurttemberg, DE	Develop Specifications But Do Not Manufacture At This Facility	View Details
3030191221	Xenios AG	Reutlingen Baden-Wurttemberg, DE	Develop Specifications But Do Not Manufacture At This Facility	View Details

510(k) Premarket Notifications (0)

No 510(k) notifications found for this entity.

FDA Recall History (0)

No recall records found for this entity.

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