Tio-H Digital Radiography Sensor

FDA 510(k) K153144 · Denttio, Inc.

Substantially Equivalent

510(k) numberK153144

Submission

Device name
Tio-H Digital Radiography Sensor
Applicant
Denttio, Inc.
Los Angeles, CA, US
Received
October 30, 2015
Decision date
February 10, 2016
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) statement available from FDA

Official FDA 510(k) record

Device classification

Product code
MUH – System, X-Ray, Extraoral Source, Digital
Device class
Class II (moderate risk)
Regulation
21 CFR 872.1800
Specialty
Dental

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K251206Digital X-Ray DentiMax Pro Imaging SystemMUH · Traditional Dentimax, Inc.09/24/2025SE
K240040VistaPano S Ceph 2.0 (VistaPano S Ceph); VistaPano S 2.0 (VistaPano S); ProVecta S-Pan…MUH · Traditional VATECH Co., Ltd.10/25/2024SE
K242778X Sensor (Model: IOS-A15IF, HDI-15DGF)MUH · Special Qpix Solutions, Inc.10/11/2024SE
K241649DUO1 and DUO2MUH · Traditional Zinnovi, Inc.07/05/2024SE
K232325RAYSCAN a-ExpertMUH · Traditional Ray Co., Ltd.04/18/2024SE
K231660Digital image scanner of dentalMUH · Traditional Jiangsu Dynamic Medical Technology Co., Ltd.12/20/2023SE
K233053DEXIS Ti2 Intraoral Sensor, DEXIS IXS Size 1 Intraoral Sensor, DEXIS IXS Size 2…MUH · Traditional Dental Imaging Technologies Corporation11/21/2023SE

Questions and answers

When was Tio-H Digital Radiography Sensor cleared by the FDA?

Tio-H Digital Radiography Sensor (K153144) received a 510(k) decision of Substantially Equivalent on February 10, 2016, 103 days after the submission was received.

What is the product code of K153144?

The FDA product code is MUH – System, X-Ray, Extraoral Source, Digital, a Class II (moderate risk) device regulated under 21 CFR 872.1800.