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FeverScan M116

by Lcr Hallcrest, LLC.

FeverScan M116 is a Class II device made by Lcr Hallcrest, LLC., listed in FDA GUDID since 24 Sep 2016 (UDI-DI 10815236020770), 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 Number10815236020770 UDI-DI Date24 Sep 2016ListedStatusListed 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  • Withdrawn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
FeverScan
Generic name
Liquid-crystal patient thermometer, reusable
Model / Ref / Catalog
M116
Primary DI / UDI-DI
10815236020770
FDA product code
KPD
GMDN term
Liquid-crystal patient thermometer, reusable
Device class
Class II
Regulation number
880.2200
GUDID distribution status
In Commercial Distribution

Similar devices

Other devices filed under FDA product code KPD (Strip, Temperature, Forehead, Liquid Crystal).

Other devices from Lcr Hallcrest, LLC.

See all devices from Lcr Hallcrest, LLC. →

Properties

  • Premarket exempt
  • Lot / batch number
Other properties (13, all answered No)