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Data / Medical devices / Switzerland / Apr Applied Pharma Research S.A.

Apr Applied Pharma Research S.A.: FDA-registered device maker in Balerna Ticino, Switzerland, 1 510(k) clearance

Apr Applied Pharma Research S.A. is registered with the FDA (registration 3003185698) in Balerna Ticino, Switzerland. It lists 1 device type. The FDA files 1 510(k) clearance under its listings, the newest dated December 22, 2015. Registered through 2026. FDA data exported November 2, 2026.

SpecStream is the live web data engine for teams and agents. It reads the FDA registration and listing, 510(k), PMA, recall and enforcement files from openFDA every week, and this page is that reading, joined by the FDA's own numbers. Ask for the makers of any device type in any country and new clearances, approvals and recalls arrive in your sheet, CRM, Slack or agent as the FDA publishes them.

FDA registration number
3003185698
Address
Via Corti 5, Balerna Ticino, Switzerland, 6828
Owner or operator
APR Applied Pharma Research s.a. (10050932)
Roles
Specification developer
First device listed
January 19, 2016
Registered through
2026
Brand names listed
Nexodyn Antimicrobial Wound Care Solution

Devices it lists

DeviceProduct codeClassRoleSource
Dressing, Wound, DrugFROUSpecification developeraccessdata.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
December 22, 2015K151168Nexodyn AOS Wound Care SolutionFROSubstantially EquivalentApr Applied Pharma Research SAaccessdata.fda.gov

Compare with other makers

Updated December 22, 2015. 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.