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iCE Surgical Light iCE30m

by Amico Clinical Solutions Corp 490 variants

iCE Surgical Light iCE30m (C14D433K) is a Class II device made by Amico Clinical Solutions Corp, listed in FDA GUDID since 14 Oct 2020 (UDI-DI 00684706003505), 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 Number00684706003505 UDI-DI Date14 Oct 2020ListedStatusListed 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  • Withdrawn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
iCE Surgical Light
Generic name
Operating room light
Model / Ref / Catalog
iCE30m, C14D433K
Primary DI / UDI-DI
00684706003505
FDA product code
FSY
GMDN term
Operating room light
Device class
Class II
Regulation number
878.4580
GUDID distribution status
In Commercial Distribution

Similar devices

Other devices filed under FDA product code FSY (Light, Surgical, Ceiling Mounted).

Other devices from Amico Clinical Solutions Corp

See all devices from Amico Clinical Solutions Corp →

Properties

  • Convenience kit
  • Serial number
  • Manufacturing date
Other properties (12, all answered No)