Skip to content

Healthlight HL-180-S

by Healthlight LLC

Healthlight HL-180-S (502025) is a Class II device made by Healthlight LLC, listed in FDA GUDID since 4 May 2017 (UDI-DI 00858935006174), registry data as of 22 Oct 2026.

Listed FDA GUDID listing, no authorization on record

Valid until

Not applicable

Database listing, no authorization

FDA recalls

Not checked

No FDA submission to match recalls against

Documents

None

No authorization documents

Trust

Unverified

Source GUDID, synced 22 Oct 2026.

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number00858935006174 UDI-DI Date4 May 2017ListedStatusListed GUDID: in commercial distribution

Official records

Coverage

1 jurisdiction

United States of America
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

United States — GUDID listing Listed

Specification

GUDID

Trade name
Healthlight
Generic name
Musculoskeletal infrared phototherapy unit, non-wearable
Model / Ref / Catalog
HL-180-S, 502025
Primary DI / UDI-DI
00858935006174
FDA product code
ILY
GMDN term
Musculoskeletal infrared phototherapy unit, non-wearable
Device class
Class II
Regulation number
890.5500
GUDID distribution status
In Commercial Distribution

Related devices

Category: Musculoskeletal infrared phototherapy unit, non-wearable

Similar devices

Other devices filed under FDA product code ILY (Lamp, Infrared, Therapeutic Heating).

Other devices from Healthlight LLC

See all devices from Healthlight LLC →

Properties

  • Over-the-counter
  • Serial number
  • Manufacturing date
Other properties (12, all answered No)