EU → North America Device Access

Flexor S.A.

ES-MF-000042891 · Spain · Barbera del Valles

Flexor S.A. is registered in the European database on medical devices as a manufacturer, with 55 devices declared. It was not found in the U.S. FDA device establishment register.

What this manufacturer declares

Class IIa55

Most frequent device types declared: FLEXOR MEDICAL CARE ESPOLÓN CALCÁNEO, FLEXOR MEDICAL CARE FASCITIS PLANTAR, FLEXOR MEDICAL CARE METATARSALGIA, FLEXOR MEDICAL CARE PIE CAVO, FLEXOR MEDICAL CARE PIE DIABÉTICO.

Among these devices, 1 are declared with a measuring function.

Devices declared under this manufacturer

Showing 12 of 55 declared devices.

Catalogue references include 1001, 1091.500 G, 1096.500 M, FM2 220 37/38, FM2 220 39/40, FM5 250 41/42.

European nomenclature codes declared: Y061203, Z1399.

United States market access

FDA establishment registerNot found in the FDA register
Devices in EUDAMED55
Country of registrationSpain

⚠️ Not found is not the same as not sold — how this comparison can be wrong.

Device-level evidence

Devices with a numeric GTIN55
Found in the U.S. device database0
Share0.0 %

Canadian market access

Health Canada licence listingNot found in the Canadian register

⚠️ Canada lists no Class I devices at all — what that excludes.

North American profile: Neither register. Flexor S.A. was not found in either the U.S. or the Canadian register.

Other manufacturers in Spain

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