FDA Device Entity Profile: VITROLIFE AB

Known Identifiers & Locations

FEI Numbers 3002757762, 3003274090, 3003995932

Owner Operator Numbers 9037178

Locations Covered Englewood, CO, US; San Diego, CA, US; Vastra Frolunda Vastra Gotaland, SE

Registered Establishments (3)

Registration #	Establishment Name	Location	Establishment Type(s)	Action
2031824	Vitrolife Inc.	San Diego, CA, US	Manufacture Medical Device	View Details
3003274090	Vitrolife Inc.	Englewood, CO, US	Manufacture Medical Device for Another Party (Contract Manufacturer)	View Details
3003995932	VITROLIFE SWEDEN AB	Vastra Frolunda Vastra Gotaland, SE	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.

Profile Disclaimer

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