FDA Device Entity Profile: Corning Incorporated

Known Identifiers & Locations

FEI Numbers 1000110807, 1218905, 1316282, 3006847360, 3011777678

Owner Operator Numbers 1317452

Locations Covered Durham, NC, US; KENNEBUNK, ME, US; ONEONTA, NY, US; Reynosa Tamaulipas, MX; Tewksbury, MA, US

Registered Establishments (5)

Registration #	Establishment Name	Location	Establishment Type(s)	Action
1054657	Corning Incorporated Discovery Labware	Durham, NC, US	Complaint File Establishment per 21 CFR 820.198	View Details
1218905	CORNING-KENNEBUNK	KENNEBUNK, ME, US	Complaint File Establishment per 21 CFR 820.198,Manufacture Medical Device	View Details
1316282	CORNING-ONEONTA	ONEONTA, NY, US	Complaint File Establishment per 21 CFR 820.198,Manufacture Medical Device	View Details
3006847360	Corning Science Mexico	Reynosa Tamaulipas, MX	Manufacture Medical Device for Another Party (Contract Manufacturer),Complaint File Establishment per 21 CFR 820.198,Manufacture Medical Device	View Details
3011777678	CORNING INCORPORATED	Tewksbury, MA, US	Complaint File Establishment per 21 CFR 820.198	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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