FDA Device Entity Profile: REPROLIFE INC.

Known Identifiers & Locations

FEI Numbers 3013019894, 3015522136, 3016927399

Owner Operator Numbers 10054077, 10060630, 10073837

Locations Covered Numazu Shizuoka, JP; Shinjuku-ku Tokyo, JP; Sumida-ku Tokyo, JP

Registered Establishments (3)

Registration #	Establishment Name	Location	Establishment Type(s)	Action
3013019894	REPROLIFE INC.	Shinjuku-ku Tokyo, JP	Complaint File Establishment per 21 CFR 820.198,Manufacture Medical Device	View Details
3015522136	KANTO GOSEI KOGYO CO.,LTD.	Sumida-ku Tokyo, JP	Manufacture Medical Device	View Details
3016927399	Omura Kogyo Co., Ltd. Hara Factory	Numazu Shizuoka, JP	Manufacture Medical Device,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.

Profile Disclaimer

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