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FondCircle FTM-D1

by FondCircle Inc.

FondCircle FTM-D1 is a Class II device made by FondCircle Inc., listed in FDA GUDID since 14 Jan 2025 (UDI-DI 00850070979177), 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 Number00850070979177 UDI-DI Date14 Jan 2025ListedStatusListed 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  • Withdrawn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
FondCircle
Generic name
Infrared patient thermometer, ear/skin
Model / reference
FTM-D1
Primary DI / UDI-DI
00850070979177
FDA product code
FLL
GMDN term
Infrared patient thermometer, ear/skin
Device class
Class II
Regulation number
880.2910
GUDID distribution status
In Commercial Distribution

Related devices

Category: Infrared patient thermometer, ear/skin

Similar devices in this category

Other devices filed under Infrared patient thermometer, ear/skin.

Other devices from FondCircle Inc.

See all devices from FondCircle Inc. →

Properties

  • Lot / batch number
  • Manufacturing date
Other properties (13, all answered No)