FDA Device Entity Profile: Sakura Global Holding Company

Known Identifiers & Locations

FEI Numbers 1000303355, 2083544, 3002689354, 3007419242

Owner Operator Numbers 8031662

Locations Covered Alphen aan den Rijn Zuid-Holland, NL; CHIKUMA-CITY Nagano, JP; TORRANCE, CA, US; Tokyo, JP

Registered Establishments (4)

Registration #	Establishment Name	Location	Establishment Type(s)	Action
1000303355	SAKURA SEIKI CO., LTD.	CHIKUMA-CITY Nagano, JP	Manufacture Medical Device	View Details
2083544	SAKURA FINETEK U.S.A., INC.	TORRANCE, CA, US	Complaint File Establishment per 21 CFR 820.198,Manufacture Medical Device	View Details
9614585	SAKURA FINETEK EUROPE B.V.	Alphen aan den Rijn Zuid-Holland, NL	Export Device to the United States But Perform No Other Operation on Device,Manufacture Medical Device	View Details
9680927	SAKURA FINETEK JAPAN CO., LTD	Tokyo, JP	Export Device to the United States But Perform No Other Operation on Device	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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