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Data / Medical devices / Liechtenstein / Bonyf AG

Bonyf AG: FDA-registered device maker in Vaduz, Liechtenstein, 1 510(k) clearance

Bonyf AG is registered with the FDA (registration 8020152) in Vaduz, Liechtenstein. It lists 5 device types. The FDA files 1 510(k) clearance under its listings, the newest dated June 2, 2006. Registered through 2026. FDA data exported November 2, 2026.

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FDA registration number
8020152
FEI number
6036
Address
Heiligkreuz 16, Vaduz, Liechtenstein, FL-9490
Owner or operator
BONYF AG (9044823)
Roles
Manufacturer
First device listed
March 1, 2001
Registered through
2026
Brand names listed
DENTTACH COMFORT Denture Relining Cushion, Denture Adhesive Cream superior (DENTTACH CLASSIC - DENTTACH FRESH), HeelFix/FingerFix Paste for cracks on heels & fingers, NitrAdine Disinfecting Tablets - DENTTACH CLEAN, OlivaFix Denture Adhesive Cream (DENTTACH GREEN - DENTTACH GREEN FRESH), OlivaFix Gold Denture Adhesive Cream - DENTTACH Gold, bandage, liquid, skin protectant, cushion, denture, over the counter

Devices it lists

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
June 2, 2006K051342MEDICAL INTERPOROUSEFTSubstantially EquivalentBonyf AGaccessdata.fda.gov

Compare with other makers

Updated June 2, 2006. 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.