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LuM-1000

by Digital Doc LLC

LuM-1000 is a Class I device made by Digital Doc LLC, listed in FDA GUDID since 21 Jan 2025 (UDI-DI 00813557020120), 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 Number00813557020120 UDI-DI Date21 Jan 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  • Withdrawn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
LuM
Generic name
LED dental light, battery-powered
Model / Ref / Catalog
LuM-1000
Primary DI / UDI-DI
00813557020120
FDA product code
EAZ
GMDN term
LED dental light, battery-powered
Device class
Class I
Regulation number
872.4630
GUDID distribution status
In Commercial Distribution

Similar devices

Other devices filed under FDA product code EAZ (Light, Operating, Dental).

Other devices from Digital Doc LLC

  • Iris-1000

    Class I
  • LuM-3000

    Class I
  • Pxl-1000

    Class I
  • Iris X90

    Class I

See all devices from Digital Doc LLC →

Properties

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