Not currently registered with FDA under this name

Zelegent, Inc.

La Jolla, CA, United States. Named as applicant on 2 dental 510(k) clearances between 2018 and 2022. 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: 22018–2022
Markets registered in: 1United States
Establishments: 0—

510(k) clearances per year, 2007–2026

510(k) clearances

Clearances on which FDA names Zelegent, Inc. as the applicant.

Decided	510(k)	Device	Device type
27 Jan 2022	K213475	Elevo Snoring Intervention Set	LRK Anti-Snoring Device
6 Dec 2018	K181107	Elevo® Kit Snoring Intervention Device	LRK Anti-Snoring Device

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.