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LightBeam LB08-Refill

by Ear Technology Corporation

LightBeam LB08-Refill is an ENT illuminating foreign body extraction set (FDA Class I; FDA product code JYG, Curette, Ear) made by Ear Technology Corporation, listed in FDA GUDID since 9 May 2022 (UDI-DI 00810323001888), 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 Number00810323001888 UDI-DI Date9 May 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  • Withdrawn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
LightBeam
Generic name
ENT illuminating foreign body extraction set
Model / reference
LB08-Refill
Primary DI / UDI-DI
00810323001888
FDA product code
JYG
GMDN term
ENT illuminating foreign body extraction set
Device class
Class I
Regulation number
874.4420
GUDID distribution status
In Commercial Distribution

Related devices

Category: Endaural wax extraction curetteENT illuminating foreign body extraction set

Similar devices

Other devices filed under FDA product code JYG (Curette, Ear).

Other devices from Ear Technology Corporation

See all devices from Ear Technology Corporation →

Properties

  • Single use
  • Convenience kit
  • Premarket exempt
Other properties (12, all answered No)