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Pico LED RX1

by Ecleris

Pico LED RX1 (LED020/2) is a Class I device made by Ecleris, listed in FDA GUDID since 27 Jan 2025 (UDI-DI B366LED0202), 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 NumberB366LED0202 UDI-DI Date27 Jan 2025ListedStatusListed GUDID: in commercial distribution

Coverage

1 jurisdiction

United States of America
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

United States — GUDID listing Listed

Specification

GUDID

Trade name
Pico LED
Generic name
LED dental light, battery-powered
Model / Ref / Catalog
RX1, LED020/2
Primary DI / UDI-DI
B366LED0202
FDA product code
KYT
GMDN term
LED dental light, battery-powered
Device class
Class I
Regulation number
880.6350
GUDID distribution status
In Commercial Distribution

Similar devices

Other devices filed under FDA product code KYT (Light, Examination, Medical, Battery Powered).

Other devices from Ecleris

See all devices from Ecleris →

Properties

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