FDA Device Entity Profile: botiss biomaterials GmbH

Known Identifiers & Locations

FEI Numbers 3014206569, 3015131160

Owner Operator Numbers 10058419

Locations Covered Dieburg Hesse, DE; Zossen Brandenburg, DE

Registered Establishments (2)

Registration #	Establishment Name	Location	Establishment Type(s)	Action
3014206569	BOTISS BIOMATERIALS GMBH	Zossen Brandenburg, DE	Develop Specifications But Do Not Manufacture At This Facility,Export Device to the United States But Perform No Other Operation on Device,Complaint File Establishment per 21 CFR 820.198	View Details
3015131160	mebios GmbH	Dieburg Hesse, DE	Manufacture Medical Device for Another Party (Contract Manufacturer)	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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