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CAPRON PODOLOGIE

FR-MF-000000322 · France · ECUISSES

CAPRON PODOLOGIE is registered in the European database on medical devices as a manufacturer, with 60 devices declared. It was not found in the U.S. FDA device establishment register.

What this manufacturer declares

Class IIa60

Most frequent device types declared: FEET PRINT, MOBI, PODOBAROSCOPE, PODOGRAPH', Réf : 13002-001 n°1, n°2, n°3, n°5, n°8, n°10, n°12.

Among these devices, 1 are declared sterile, 40 active.

Devices declared under this manufacturer

Showing 12 of 60 declared devices.

Catalogue references include 0142, 10790-BL, 10840E-CP-D, 10840MA-CP-G, 13002, 6057.

European nomenclature codes declared: V9099, V010302.

United States market access

FDA establishment registerNot found in the FDA register
Devices in EUDAMED60
Country of registrationFrance

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

Device-level evidence

Devices with a numeric GTIN59
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. CAPRON PODOLOGIE was not found in either the U.S. or the Canadian register.

Other manufacturers in France

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