FDA Device Entity Profile: Corflex Global, LLC

Known Identifiers & Locations

FEI Numbers 1218997, 3010621943

Owner Operator Numbers 1218997

Locations Covered MANCHESTER, NH, US; Santo Domingo Este, DO

Registered Establishments (2)

Registration #	Establishment Name	Location	Establishment Type(s)	Action
1218997	CORFLEX	MANCHESTER, NH, US	Complaint File Establishment per 21 CFR 820.198,Repack or Relabel Medical Device,Manufacture Medical Device,Manufacture Medical Device for Another Party (Contract Manufacturer)	View Details
3010621943	Corflex Caribe	Santo Domingo Este, DO	Complaint File Establishment per 21 CFR 820.198,Manufacture Medical Device for Another Party (Contract Manufacturer),Repack or Relabel Medical Device,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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