LifeLens Physiological Monitor
FDA 510(k) K260157 · LifeLens Technologies, Inc.
510(k) numberK260157
Submission
- Device name
- LifeLens Physiological Monitor
- Applicant
- LifeLens Technologies, Inc.
Ivyland, PA, US - Received
- January 20, 2026
- Decision date
- July 9, 2026
- Decision
- Substantially Equivalent (SESE)
- Type
- Traditional 510(k)
- Summary
- 510(k) summary available from FDA
Device classification
- Product code
- DSH – Recorder, Magnetic Tape, Medical
- Device class
- Class II (moderate risk)
- Regulation
- 21 CFR 870.2800
- Specialty
- Cardiovascular
Other 510(k)s with product code DSH
| 510(k) | Device | Applicant | Decision |
|---|---|---|---|
| K252389 | Rhythm Master ECG Patch (HM-15BB-AX, HM-15BW-AX, HM-15BW-DX)DSH · Traditional | Smwmed, Inc. | 04/23/2026SE |
| K253293 | VitaloJAK Clinic (Model 7100)DSH · Special | Vitalograph , Ltd. | 12/03/2025SE |
| K243650 | Zio® monitor (DFG0001)DSH · Traditional | iRhythm Technologies, Inc. | 08/15/2025SE |
| K243603 | AeviceMDDSH · Traditional | Aevice Health Pte. , Ltd. | 05/05/2025SE |
| K242583 | AT-Patch (ATP-C130/ATP-C70)DSH · Traditional | Atsens Co., Ltd. | 05/02/2025SE |
| K232670 | HiCardi+ H100DSH · Traditional | MEZOO Co., Ltd. | 09/20/2024SE |
| K233906 | S-Patch (S-Patch ExL)DSH · Special | Wellysis Corp. | 02/16/2024SE |
| K231104 | ABPMproDSH · Traditional | Somnomedics GmbH | 11/27/2023SE |
| K233110 | Carnation Ambulatory MonitorDSH · Traditional | Bardy Diagnostics, Inc. | 11/22/2023SE |
| K230184 | Holter ECG and ABP SystemDSH · Traditional | Edan Instruments, Inc. | 09/25/2023SE |
More from Edan Instruments, Inc.
| 510(k) | Device | Decision |
|---|---|---|
| K203168 | LifeLens Wireless ECG MonitorDSH · Traditional | 07/20/2021SE |
Questions and answers
When was LifeLens Physiological Monitor cleared by the FDA?
LifeLens Physiological Monitor (K260157) received a 510(k) decision of Substantially Equivalent on July 9, 2026, 170 days after the submission was received.
What is the product code of K260157?
The FDA product code is DSH – Recorder, Magnetic Tape, Medical, a Class II (moderate risk) device regulated under 21 CFR 870.2800.