Manufacturer registered with FDA

Diamond Orthotic Laboratory, LLC

La Mesa, CA, United States. Lists 1 dental device type with FDA across 1 registered establishment, and holds 1 510(k) clearance as applicant.

FDA owner/operator10059263Contract manufacturerManufacturer

Device types listed: 1
Brands and models: 2
510(k) clearances: 12020–2020
Markets registered in: 1United States
Establishments: 1United States

510(k) clearances per year, 2007–2026

Devices listed with FDA

What Diamond Orthotic Laboratory, LLC currently lists, by FDA device type, with the brand and model names on the listing.

Device type	Category	Role	Brands and models	Listed since
Anti-Snoring DeviceLRK · Class 2	Anti-snoring & jaw-repositioning devices	Maker	DDSO (Diamond Digital Sleep Orthotic)SnoreHook	2018

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

510(k) clearances

Clearances on which FDA names Diamond Orthotic Laboratory, LLC as the applicant.

Decided	510(k)	Device	Device type
3 Sep 2020	K202499	Diamond Digital Sleep Orthotic (DDSO)	LRK Anti-Snoring Device

Registered establishments

Establishment	Location	What it does
DIAMOND ORTHOTIC LABORATORY, LLCFDA reg. 3012728846	La Mesa, CA, United States	Contract manufacturer, Manufacturer

Sources

FDA establishment registration & device listing (search FDA, owner/operator 10059263). 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.