Forehead Thermometer JPD-FR200

by Shenzhen Yihao Technology Co., Ltd

Listed FDA GUDID listing, no authorization on record

Valid until

Not applicable

Database listing, no authorization

FDA recalls

in data synced 22 Oct 2026

Documents

None

No authorization documents

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source GUDID, synced 22 Oct 2026. What this means

Regulatory status

as of registry sync 22 Oct 2026

Region	Authorization	Number	Date	Status
United States	GUDID listing	Number06970596810014 UDI-DI	Date15 Sep 2016Listed	StatusListed GUDID: in commercial distribution

Recalls

0 recalls · FDA

No FDA recalls found in the data synced 22 Oct 2026.

Coverage

1 jurisdiction

Active
Expiring
Withdrawn
Listed
Not covered

United States — GUDID listing Listed

Specification

GUDID

Trade Name: Forehead Thermometer
Generic Name: Infrared patient thermometer, skin
Model / Reference: JPD-FR200

Primary DI / UDI-DI: 06970596810014
510(k) Number: K131243
FDA Product Code: FLL
GMDN Term: Infrared patient thermometer, skin

Device Class: Class II
Regulation Number: 880.2910
GUDID distribution status: In Commercial Distribution

Properties

Lot / Batch Number
Serial Number

Other properties (12)

Sterile: No
Single Use: No
Implantable: No
Contains Latex: No
Prescription Use: No
Over-the-Counter: No
Convenience Kit: No
Combination Product: No
HCT/P: No
Premarket Exempt: No
Expiration Date: No
Manufacturing Date: No