FDA Device Entity Profile: CeramTec GmbH

Known Identifiers & Locations

FEI Numbers 3001278222, 3002806653, 3008886124

Owner Operator Numbers 9066049

Locations Covered Lauf an der Pegnitz Bavaria, DE; MARKTREDWITZ Bavaria, DE; PLOCHINGEN Baden-Wurttemberg, DE

Registered Establishments (3)

Registration #	Establishment Name	Location	Establishment Type(s)	Action
3001278222	CERAMTEC GmbH Medical Products Division	MARKTREDWITZ Bavaria, DE	Manufacture Medical Device for Another Party (Contract Manufacturer)	View Details
3008886124	CERAMTEC GMBH	Lauf an der Pegnitz Bavaria, DE	Manufacture Medical Device for Another Party (Contract Manufacturer)	View Details
8044172	CERAMTEC GmbH Medical Products Division	PLOCHINGEN Baden-Wurttemberg, 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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