FDA Device Entity Profile: BONART CO. LTD.

Known Identifiers & Locations

FEI Numbers 3008981576

Owner Operator Numbers 9039893

Locations Covered KEELUNG, TW

Registered Establishments (1)

Registration #	Establishment Name	Location	Establishment Type(s)	Action
9710363	BONART CO. LTD.	KEELUNG, TW	Manufacture Medical Device,Manufacture Medical Device for Another Party (Contract Manufacturer)	View Details

510(k) Premarket Notifications (1)

Submission #	Device Name	Decision Date	Decision Description	Action
K994299	ART-P3, MODEL P3-1-ART-A1	2000-03-06	Substantially Equivalent	View Details

FDA Recall History (0)

No recall records found for this entity.

Profile Disclaimer

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