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Boost LED Collar TN2113

by iSMART Developments, Ltd.

Boost LED Collar TN2113 (150-LS) is a Class II device made by iSMART Developments, Ltd., listed in FDA GUDID since 19 Oct 2022 (UDI-DI 05060534510494), 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 Number05060534510494 UDI-DI Date19 Oct 2022ListedStatusListed 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  • Withdrawn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
Boost LED Collar
Generic name
Red/infrared light phototherapy unit
Model / Ref / Catalog
TN2113, 150-LS
Primary DI / UDI-DI
05060534510494
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

Similar devices

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

Other devices from iSMART Developments, Ltd.

See all devices from iSMART Developments, Ltd. →

Properties

  • Over-the-counter
  • Premarket exempt
  • Lot / batch number
  • Serial number
  • Manufacturing date
Other properties (10, all answered No)