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Lescolton Ls-30500

by Shenzhen Lescolton Medical Equipment Co., Ltd.

Lescolton Ls-30500 is a Class II device made by Shenzhen Lescolton Medical Equipment Co., Ltd., listed in FDA GUDID since 16 Sep 2025 (UDI-DI 06977003800316), 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 Number06977003800316 UDI-DI Date16 Sep 2025ListedStatusListed 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  • Withdrawn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
Lescolton
Generic name
Blue/red/infrared phototherapy lamp
Model / reference
LS-30500
Primary DI / UDI-DI
06977003800316
FDA product code
ILY
GMDN term
Blue/red/infrared phototherapy lamp
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 Shenzhen Lescolton Medical Equipment Co., Ltd.

See all devices from Shenzhen Lescolton Medical Equipment Co., Ltd. →

Properties

  • Over-the-counter
  • Premarket exempt
  • Lot / batch number
  • Serial number
Other properties (11, all answered No)