FDA Device Entity Profile: NIPRO VASCULAR CORPORATION

Known Identifiers & Locations

FEI Numbers 1000533027, 3007835716, 3011826338, 3030042169

Owner Operator Numbers 10061300

Locations Covered Nagoya Aichi, JP; Seto Aichi, JP

Registered Establishments (4)

Registration #	Establishment Name	Location	Establishment Type(s)	Action
1000533027	NIPRO VASCULAR CORPORATION Fujigaoka Building	Nagoya Aichi, JP	Complaint File Establishment per 21 CFR 820.198	View Details
3007835716	NIPRO VASCULAR CORPORATION	Nagoya Aichi, JP	Manufacture Medical Device	View Details
3011826338	NIPRO VASCULAR CORPORATION Seto Facility / NIPRO VASCULAR CORPORATION Innovation Center	Seto Aichi, JP	Develop Specifications But Do Not Manufacture At This Facility	View Details
3030042169	NIPRO VASCULAR CORPORATION Aichi Facility	Seto Aichi, JP	Manufacture Medical 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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