Not currently registered with FDA under this name

Theodent, LLC

New Orleans, LA, United States. Named as applicant on 1 dental 510(k) clearance between 2025 and 2025. No establishment is registered with FDA under this exact name today.

1 clearance in five years

Device types listed: 0
Brands and models: 0
510(k) clearances: 12025–2025
Markets registered in: 1United States
Establishments: 0—

510(k) clearances per year, 2007–2026

510(k) clearances

Clearances on which FDA names Theodent, LLC as the applicant.

Decided	510(k)	Device	Device type
27 May 2025	K243777	Rennou Varnish (3% / Spearmint); Rennou Varnish (3% / Strawberry); Rennou Varnish (3% / Cherry); Rennou Varnish (3% / Bubble Gum)	LBH Cavity Varnish

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.