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Benilight iLED-Pro

by Benilight

Benilight iLED-Pro is a Class II device made by Benilight, listed in FDA GUDID since 1 Oct 2024 (UDI-DI 08809922440039), registry data as of 23 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 23 Oct 2026.

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number08809922440039 UDI-DI Date1 Oct 2024ListedStatusListed 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  • Withdrawn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
Benilight
Generic name
Red/infrared light phototherapy unit
Model / reference
iLED-Pro
Primary DI / UDI-DI
08809922440039
FDA product code
ILY
GMDN term
Red/infrared light phototherapy unit
Device class
Class II
Regulation number
890.5500
GUDID distribution status
In Commercial Distribution

Related devices

Category: Red/infrared light phototherapy unit

Similar devices

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

Other devices from Benilight

Properties

  • Over-the-counter
  • Premarket exempt
  • Serial number
  • Manufacturing date
Other properties (11, all answered No)