FDA Device Entity Profile: KLS Martin SE & Co. KG

Known Identifiers & Locations

FEI Numbers 1000525271, 1000614294, 3002807464, 3014201171, 3036795921

Owner Operator Numbers 10089006

Locations Covered Freiburg Baden-Wurttemberg, DE; Fridingen Baden-Wurttemberg, DE; Jacksonville, FL, US; Muhlheim/Donau Baden-Wurttemberg, DE; Simpang Ampat Pulau Pinang, MY

Registered Establishments (5)

Registration #	Establishment Name	Location	Establishment Type(s)	Action
1057946	KLS-Martin L.P.	Jacksonville, FL, US	Develop Specifications But Do Not Manufacture At This Facility	View Details
3014201171	KLS Martin Malaysia Sdn. Bhd.	Simpang Ampat Pulau Pinang, MY	Manufacture Medical Device for Another Party (Contract Manufacturer)	View Details
3036795921	KLS MARTIN SE & CO. KG	Fridingen Baden-Wurttemberg, DE	Manufacture Medical Device for Another Party (Contract Manufacturer)	View Details
9610905	KLS Martin SE & Co. KG	Muhlheim/Donau Baden-Wurttemberg, DE	Manufacture Medical Device for Another Party (Contract Manufacturer)	View Details
9681383	KLS Martin SE & Co. KG	Freiburg Baden-Wurttemberg, DE	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.

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