Prosthetic devices · 21 CFR 872 Subpart D

Carboxymethylcellulose Sodium (32%) and Ethylene-Oxide Homopolymer Denture Adhesive

FDA device type “Adhesive, Denture, Carboxymethylcellulose Sodium (32%) And Ethylene-Oxide Homopolymer”.

FDA codeKOLClass121 CFR872.3410Pathway510(k) exempt
Companies listing it
75 makers
Brands and models
7
510(k) clearances
20 in five years
FDA name
Adhesive, Denture, Carboxymethylcellulose Sodium (32%) And Ethylene-Oxide Homopolymer
1979: 11989: 119801990200020102020

510(k) clearances per year, 1976–2026

Companies that list KOL

7 companies currently list this device type with FDA.

CompanyCountryRoleBrands and models listedClearancesLatest
bredent GmbH & Co. KGGermanyMaker—32024
Prestige Brands Holdings, Inc.United StatesMakerEffergrip12013
HaleonUnited StatesMakerPOLIGRIP DENTURE ADHESIVE · Poligrip Power Max Ultimate All in 1——
Kyowa LimitedJapanMakerPOLIGRIP COMFORT STRIPS · POLYGRIP COMFORT STRIPS——
Scapa Tapes North America LLCUnited StatesMaker———
Dentimed Sao Joao LLCUnited StatesRepacker / relabelerTOSCANA——
WestRock Converting, LLCUnited StatesRepacker / relabelerPoligrip Cushion Comfort; Poligrip Max Seal Denture Adhesive; Poligrip Super Denture Adhesive——

510(k) clearances

Decided510(k)DeviceApplicant
24 Feb 1989K884999HOLD-FAST DENTURE ADHESIVEIodent, Co.
26 Oct 1979K791576FORGET - DENTURE BONDING LIQUIDNorcliff Thayer, Inc.

Official records: FDA product classification for KOL · 21 CFR 872.3410.

Source: FDA establishment registration & device listing, 510(k) and product classification files · FDA data as of 2 Nov 2026 · snapshot 12 Nov 2026