FDA Registration Number: 3008880500

Last Validated: August 11, 2022

Status: Valid

Valid2022 U.S. FDA Medical Device Establishment Registration

ASKORN MEDICAL

Establishment Information

44c rue de Bray
Cesson Sevigne Bretagne, FR F-35510

U.S. Agent and Official Correspondent

Registrar Corp
144 Research Drive
Hampton VA, USA 23666
Registration of a device establishment, assignment of a registration number, or listing of a medical device does not in any way denote approval of the establishment or its products by U.S. FDA.

Listings on file with FDA

Device Name Product Code Status Last Validated  
Retractor GAD Valid August 10, 2022

Device Listing

Device Name

Retractor

Product Code

GAD

Company Function(s)

Specification Developer, Foreign Exporter

Proprietary Name(s)

Cannulated Compressor PFCC
Oxford Concise MCL Retractor
Support, Patient Position CCX Valid August 10, 2022

Device Listing

Device Name

Support, Patient Position

Product Code

CCX

Company Function(s)

Foreign Exporter, Specification Developer

Proprietary Name(s)

Knee Positioning Device
OSSKAR

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