FDA Registration Number: 8020152

Last Validated: June 11, 2026

Status: Valid

Valid2026 U.S. FDA Medical Device Establishment Registration

BONYF AG

Establishment Information

HEILIGKREUZ 16
VADUZ, LI FL-9490

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  
Cleanser, Denture, Over The Counter EFT Valid June 10, 2026

Device Listing

Device Name

Cleanser, Denture, Over The Counter

Product Code

EFT

Company Function(s)

Manufacturer

Proprietary Name(s)

Cushion, Denture, Over The Counter EHS Valid June 10, 2026

Device Listing

Device Name

Cushion, Denture, Over The Counter

Product Code

EHS

Company Function(s)

Manufacturer

Proprietary Name(s)

Carboxymethylcellulose Sodium Or Polyvinyl Methylether Maleic Acid Calcium-Sodium KOT Valid June 10, 2026

Device Listing

Device Name

Carboxymethylcellulose Sodium Or Polyvinyl Methylether Maleic Acid Calcium-Sodium

Product Code

KOT

Company Function(s)

Manufacturer

Proprietary Name(s)

Bandage, Liquid, Skin Protectant NEC Valid June 10, 2026

Device Listing

Device Name

Bandage, Liquid, Skin Protectant

Product Code

NEC

Company Function(s)

Manufacturer

Proprietary Name(s)

Adhesive, Denture, Polyvinyl Methylether Maleic Acid Calcium-Sodium Double Salt KOO Valid June 10, 2026

Device Listing

Device Name

Adhesive, Denture, Polyvinyl Methylether Maleic Acid Calcium-Sodium Double Salt

Product Code

KOO

Company Function(s)

Manufacturer

Proprietary Name(s)

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