FDA Device Entity Profile: K LINE EUROPE GMBH

Known Identifiers & Locations

FEI Numbers 3033492726, 3035484470, 3044462786, 3044853366

Owner Operator Numbers 10079939

Locations Covered Cairo, EG; Chaves Braga, PT; Tijuana B.C. Baja California, MX; West Palm Beach, FL, US

Registered Establishments (4)

Registration #	Establishment Name	Location	Establishment Type(s)	Action
3033492726	K Line Portugal Unipessoal Ltd	Chaves Braga, PT	Manufacture Medical Device for Another Party (Contract Manufacturer)	View Details
3035484470	Border Assembly S. de R.L de C.V.	Tijuana B.C. Baja California, MX	Repack or Relabel Medical Device,Manufacture Medical Device	View Details
3044462786	K Line Florida	West Palm Beach, FL, US	Manufacture Medical Device	View Details
3044853366	K Line Egypt	Cairo, EG	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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