BONYF AG

FDA Device Registration & Listing · VADUZ, LI · Registration 8020152

Public Record Device Listing Expiry Year: 2026 This page presents structured fields from public FDA datasets.

Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source
FDA Device Registration & Listing
Record Type
Device registration/listing
Registration Number
8020152
FEI Number
6036
Entity Name
BONYF AG
City/State/Country
VADUZ, LI
Establishment Address
HEILIGKREUZ 16, VADUZ FL-9490, LI
Establishment Type(s)
Manufacture Medical Device
Owner / Operator
BONYF AG (Owner Number: 9044823)
Owner / Operator Contact Address
16 HEILIGKREUZ, --, VADUZ, LI-NOTA FL-9490, LI
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

Denture Adhesive Cream superior (DENTTACH CLASSIC - DENTTACH FRESH) OlivaFix Denture Adhesive Cream (DENTTACH GREEN - DENTTACH GREEN FRESH) cushion, denture, over the counter DENTTACH COMFORT Denture Relining Cushion OlivaFix Gold Denture Adhesive Cream - DENTTACH Gold

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
KOT Carboxymethylcellulose Sodium Or Polyvinyl Methylether Maleic Acid Calcium-Sodium Dental Class 1 872.3490 2001-03-01
EHS Cushion, Denture, Over The Counter Dental Class 2 872.3540 2025-07-14
KOO Adhesive, Denture, Polyvinyl Methylether Maleic Acid Calcium-Sodium Double Salt Dental Class 1 872.3490 2017-02-09

Official Correspondent

No official correspondent registered.

US Agent Details

David Lennarz Business: Registrar Corp Email: david.lennarz@registrarcorp.com Phone: (757) 2240177

Related Public Records

Same Entity

BONYF AG
View consolidated registration, premarket clearance, and recall records for this applicant.
View Entity Profile →

Related 510(k) Records

510(k) Number Applicant Device Name Decision Date
K884357 Precision Dynamics Corp. PRECISION BIOPORT COLLECTION & TRANSPORT SYSTEM 1988-11-01

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 8020152. Last updated year: 2026. Please use registration number 8020152 when referencing this establishment in official correspondence.
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