Manufacturer registered with FDA

True Function Laboratory Inc

La Mesa, CA, United States. Lists 1 dental device type with FDA across 1 registered establishment, and holds 3 510(k) clearances as applicant.

FDA owner/operator10043880Contract manufacturerManufacturer1 clearance in five years
Device types listed
1
Brands and models
3
510(k) clearances
32017–2026
Markets registered in
1United States
Establishments
1United States
2017: 12019: 12026: 120102020

510(k) clearances per year, 2007–2026

Devices listed with FDA

What True Function Laboratory Inc currently lists, by FDA device type, with the brand and model names on the listing.

Device typeCategoryRoleBrands and modelsListed since
Anti-Snoring DeviceLRK · Class 2Anti-snoring & jaw-repositioning devicesMaker
Elastic Mandibular Advancement (EMA)True Function Adjustable Herbst AppliancesTrueDorsal
2013

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 True Function Laboratory Inc as the applicant.

Decided510(k)DeviceDevice type
6 Oct 2026K260136ForzaLRK Anti-Snoring Device
11 Feb 2019K180691TrueDorsal DevicesLRK Anti-Snoring Device
24 Nov 2017K170578True Function Adjustable Herbst AppliancesLRK Anti-Snoring Device

Registered establishments

EstablishmentLocationWhat it does
TRUE FUNCTION LABORATORY INCFDA reg. 3007108578La Mesa, CA, United StatesContract manufacturer, Manufacturer

Sources

FDA establishment registration & device listing (search FDA, owner/operator 10043880). 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.