Manufacturer registered with FDA

Lucas Lifecare, LLC

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

FDA owner/operator10086032Manufacturer1 clearance in five years

Device types listed: 1
Brands and models: 1
510(k) clearances: 12024–2024
Markets registered in: 1United States
Establishments: 1United States

510(k) clearances per year, 2007–2026

Devices listed with FDA

What Lucas Lifecare, 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
Extraoral with Timer X-Ray UnitEHD · Class 2	Dental X-ray units	Maker	LifeRay Intraoral Handheld X-ray	2024

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 Lucas Lifecare, LLC as the applicant.

Decided	510(k)	Device	Device type
5 Jul 2024	K241305	LifeRay Intraoral Handheld X-ray System	EHD Extraoral with Timer X-Ray Unit

Registered establishments

Establishment	Location	What it does
LUCAS LIFECARE, LLCFDA reg. 3025308469	Janesville, WI, United States	Manufacturer

Sources

FDA establishment registration & device listing (search FDA, owner/operator 10086032). 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.