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Midmark LT-1500-126

by Midmark Corporation

Midmark LT-1500-126 is a Class I device made by Midmark Corporation, listed in FDA GUDID since 10 Mar 2026 (UDI-DI 00841709122040), 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 Number00841709122040 UDI-DI Date10 Mar 2026ListedStatusListed 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  • Withdrawn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
Midmark
Generic name
LED dental light, line-powered
Model / Ref / Catalog
LT-1500-126
Primary DI / UDI-DI
00841709122040
FDA product code
EAZ
GMDN term
LED dental light, line-powered
Device class
Class I
Regulation number
872.4630
GUDID distribution status
In Commercial Distribution
MRI safety
MR Unsafe

Similar devices

Other devices filed under FDA product code EAZ (LIGHT, OPERATING, DENTAL).

Other devices from Midmark Corporation

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Properties

  • Premarket exempt
  • Serial number
  • Manufacturing date
Other properties (12, all answered No)