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Tri Star TS2015W-E

by Sunnex, Inc.

Tri Star TS2015W-E is a fixed examination/treatment room light (FDA Class I; FDA product code KZF, Device, medical examination, ac powered) made by Sunnex, Inc., listed in FDA GUDID since 26 Feb 2018 (UDI-DI 00853538008273), 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 Number00853538008273 UDI-DI Date26 Feb 2018ListedStatusListed 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  • Withdrawn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
Tri Star
Generic name
Fixed examination/treatment room light
Model / Ref / Catalog
TS2015W-E
Primary DI / UDI-DI
00853538008273
FDA product code
KZF
GMDN term
Fixed examination/treatment room light
Device class
Class I
Regulation number
880.6320
GUDID distribution status
In Commercial Distribution

Related devices

Category: Fixed examination/treatment room light

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Other devices filed under Fixed examination/treatment room light.

Other devices from Sunnex, Inc.

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Properties

  • Premarket exempt
  • Serial number
Other properties (13, all answered No)