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Data / Medical devices / Germany / Bsn-Jobst GMBH

Bsn-Jobst GMBH: FDA-registered device maker in EMMERICH North Rhine-Westphalia, Germany, 2 510(k) clearances

Bsn-Jobst GMBH is registered with the FDA (registration 8043565) in EMMERICH North Rhine-Westphalia, Germany. It lists 3 device types. The FDA files 2 510(k) clearances under its listings, the newest dated July 10, 2013. Registered through 2026. FDA data exported November 2, 2026.

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FDA registration number
8043565
FEI number
3005588760
Address
Beiersdorfstrasse 1, EMMERICH North Rhine-Westphalia, Germany, 46446
Owner or operator
BSN medical GmbH (9047426)
Roles
Complaint file establishment, Manufacturer, Specification developer
First device listed
April 14, 2003
Registered through
2026
Brand names listed
Actimove Everyday Supports Posture Control Brace, Bellavar, Custom Seamless Soft, Elvarex, Elvarex Plus, Elvarex Soft, Elvarex Soft Seamless, Epstein Facioplasty and more

Devices it lists

DeviceProduct codeClassRoleSource
Aid, TransferIKX1Complaint file establishment, Specification developeraccessdata.fda.gov
Binder, Medical, TherapeuticMDR1Manufactureraccessdata.fda.gov
Stocking, Medical Support (To Prevent Pooling Of Blood In Legs)DWL2Complaint file establishment, Manufactureraccessdata.fda.gov

510(k) clearances

The 510(k) numbers this establishment lists, with the FDA decision on each. The applicant is the company that holds the clearance.

Decided510(k) numberDeviceProduct codeDecisionApplicantSource
July 10, 2013K131496BELLAVAR / CUSTOM SEAMLESS SOFT (A.K.A. COMTESSE)DWLSubstantially EquivalentBsn Medical, Inc.accessdata.fda.gov
December 18, 2012K123561ELVAREX/ELVAREX SOFT/ELVAREX SOFT SEAMLESSDWLSubstantially EquivalentBsn Medical, Inc.accessdata.fda.gov

Compare with other makers

Updated July 10, 2013. Read from openFDA bulk downloads (device registration and listing, 510(k), PMA, recall and enforcement files). CC0 1.0, public domain (openFDA terms of service). The files are joined on FDA identifiers: the 510(k) and PMA numbers a registration lists, and the recalling firm's FEI for recalls. Recall class comes from the FDA enforcement report. The FDA states that openFDA data is unvalidated and is not for decisions about medical care. Free to reuse with credit to SpecStream under CC BY 4.0. Spot a wrong value? Write to [email protected] with the link to this page.