EU → US 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 PIE DIABÉTICO, FLEXOR MEDICAL CARE PIE PLANO, FLEXOR MEDICAL CARE FASCITIS PLANTAR, FLEXOR MEDICAL CARE METATARSALGIA, FLEXOR MEDICAL CARE ESPOLÓN CALCÁNEO.

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

No authorised representative is recorded for these devices. For a manufacturer established outside the Union that would be unusual; for one established inside it, it is normal.

United States market access

FDA establishment registerNot found in the FDA register
Devices in EUDAMED55
Country of registrationSpain
⚠️ Absence here is not proof of absence from the market. A manufacturer may reach the United States through a distributor registered under its own name, or under a corporate name we could not match. We publish what we measured, not what we inferred.

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