Dental Device Guide
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Not currently registered with FDA under this name

Iodent, Co.

Champaign, IL, United States. Named as applicant on 1 dental 510(k) clearance between 1989 and 1989. No establishment is registered with FDA under this exact name today.

Device types listed
0
Brands and models
0
510(k) clearances
11989–1989
Markets registered in
1United States
Establishments
0—
1989: 119801990200020102020

510(k) clearances per year, 1980–2026

510(k) clearances

Clearances on which FDA names Iodent, Co. as the applicant.

Decided510(k)DeviceDevice type
24 Feb 1989K884999HOLD-FAST DENTURE ADHESIVEKOL Carboxymethylcellulose Sodium (32%) and Ethylene-Oxide Homopolymer Denture Adhesive

Sources

FDA 510(k) premarket notification file. FDA data as of 2 Nov 2026; snapshot 12 Nov 2026. The location shown is the address on FDA's record of the most recent filing, which can be a US agent.