Titan Dental Design

FDA 510(k) K232429 · Clearadvance, LLC

Substantially Equivalent

510(k) numberK232429

Submission

Device name
Titan Dental Design
Applicant
Clearadvance, LLC
Irvine, CA, US
Received
August 11, 2023
Decision date
October 13, 2023
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) summary available from FDA

Official FDA 510(k) record

Device classification

Product code
PNN – Orthodontic Software
Device class
Class II (moderate risk)
Regulation
21 CFR 872.5470
Specialty
Dental

The device is software that is to be used for the diagnosis and treatment planning of orthodontic patients and conditions. It may include orthodontic output devices used for the treatment of orthodontics. The device is intended for prescription use only.

Other 510(k)s with product code PNN

510(k)DeviceApplicantDecision
K260419LingOral Dental Design SystemPNN · Traditional Hangzhou ChohoTech Co., Ltd.05/08/2026SE
K253565SureSmile SoftwarePNN · Traditional Dentsply Sirona, Inc.03/04/2026SE
K252507SmileInspectorPNN · Traditional Amv Consulting, LLC01/07/2026SE
K253343Celebrace SoftwarePNN · Traditional Celebrace12/29/2025SE
K250198Laon OrthoPNN · Traditional Laon Medi, Inc.04/23/2025SE
K241153Progressive Orthodontics AppPNN · Traditional Progressive Aligners, Inc.10/11/2024SE
K233625Raydent SWPNN · Traditional Ray Co., Ltd.05/16/2024SE
K232564Align StudioPNN · Traditional Laon Medi, Inc.03/12/2024SE
K233616Clevaligner Software (V1.0.0)PNN · Traditional Clevaligner, Ltd.01/11/2024SE
K232549NemoCastPNN · Traditional Software Nemotec S.L.11/21/2023SE

Questions and answers

When was Titan Dental Design cleared by the FDA?

Titan Dental Design (K232429) received a 510(k) decision of Substantially Equivalent on October 13, 2023, 63 days after the submission was received.

What is the product code of K232429?

The FDA product code is PNN – Orthodontic Software, a Class II (moderate risk) device regulated under 21 CFR 872.5470.