Manufacturer registered with FDA

Crane Dental Laboratory

Rochester, NY, United States. Lists 2 dental device types with FDA across 1 registered establishment, and holds 2 510(k) clearances as applicant.

FDA owner/operator10044573Contract manufacturerManufacturer

Device types listed: 2
Brands and models: 8
510(k) clearances: 22014–2019
Markets registered in: 1United States
Establishments: 1United States

510(k) clearances per year, 2007–2026

Devices listed with FDA

What Crane Dental Laboratory 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	Crane Acrylic Herbst ApplianceEMALamberg SleepWellRespire Blue SeriesSapphire Dorsal Comfort FitSapphire Herbst ApplianceTap III Anti-Snoring Device	2013
Jaw Repositioning DeviceLQZ · Class 2	Anti-snoring & jaw-repositioning devices	Maker	Lamberg SleepWell	2014

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 Crane Dental Laboratory as the applicant.

Decided	510(k)	Device	Device type
17 Sep 2019	K181416	Sapphire Dorsal Comfort Fit	LRK Anti-Snoring Device
11 Sep 2014	K140429	CRANE ACRYLIC HERBST APPLIANCE	LRK Anti-Snoring Device

Registered establishments

Establishment	Location	What it does
CRANE DENTAL LABORATORYFDA reg. 3010324114	Rochester, NY, United States	Contract manufacturer, Manufacturer

Sources

FDA establishment registration & device listing (search FDA, owner/operator 10044573). 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.