Tyto Stethoscope (G3)

FDA 510(k) K252089 · Tyto Care , Ltd.

Substantially Equivalent

510(k) numberK252089

Submission

Device name
Tyto Stethoscope (G3)
Applicant
Tyto Care , Ltd.
Netanya, IL
Received
July 2, 2025
Decision date
March 12, 2026
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) summary available from FDA

Official FDA 510(k) record

Device classification

Product code
DQD – Stethoscope, Electronic
Device class
Class II (moderate risk)
Regulation
21 CFR 870.1875
Specialty
Cardiovascular

Other 510(k)s with product code DQD

510(k)DeviceApplicantDecision
K261494Smart Wireless Stethoscope (STEMO310);Smart Wireless Stethoscope (STEMO710);Smart…DQD · Traditional Shanghai Hulu Devices Co., Ltd.07/31/2026SE
K261694CORE 300 Digital StethoscopeDQD · Traditional Eko Health, Inc.07/23/2026SE
K252915AiSteth®DQD · Traditional Ai Health Highway India Pvt., Ltd.05/22/2026SE
K252076Kneevoice Cartilage Evaluation System (750-3600-001)DQD · Traditional Kneevoice, Inc.02/06/2026SE
K252284eMurmur Heart AIDQD · Traditional Csd Labs12/19/2025SE
K252595Stethophone ProDQD · Special Sparrow Acoustics, Inc.09/12/2025SE
K251494Eko Foundation Analysis Software with Transformers (EFAST)DQD · Traditional Eko Health, Inc.08/12/2025SE
K242971AccurSound Electronic Stethoscope (AS101)DQD · Traditional Heroic Faith International , Ltd.11/25/2024SE
K240901StethophoneDQD · Traditional Sparrow Acoustics, Inc.09/19/2024SE
K233313Keikku Electronic stethoscopeDQD · Traditional Lapsi Health Holding B.V.04/10/2024SE

More from Lapsi Health Holding B.V.

510(k)DeviceDecision
K252844Tyto Insights for Wheeze Detection (with PCCP)PHZ · Traditional 06/02/2026SE
K243567Tyto Insights for Rhonchi DetectionPHZ · Traditional 04/07/2025SE
K240555Tyto Insights for Crackles DetectionPHZ · Traditional 07/02/2024SE
K232237Tyto Insights for Wheeze DetectionPHZ · Traditional 12/13/2023SE
K221614TytoCare Lung Sounds AnalyzerPHZ · Traditional 02/24/2023SE
K190242Tyto ThermometerFLL · Traditional 03/27/2019SE
K181612Tyto Stethoscope (OTC)DQD · Traditional 12/17/2018SE
K160401Tyto StethoscopeDQD · Traditional 10/19/2016SE

Questions and answers

When was Tyto Stethoscope (G3) cleared by the FDA?

Tyto Stethoscope (G3) (K252089) received a 510(k) decision of Substantially Equivalent on March 12, 2026, 253 days after the submission was received.

What is the product code of K252089?

The FDA product code is DQD – Stethoscope, Electronic, a Class II (moderate risk) device regulated under 21 CFR 870.1875.