Data / Medical devices / United States / LifeSignals, Inc.
LifeSignals, Inc.: FDA-registered device maker in Milpitas, CA, United States, 4 510(k) clearances
LifeSignals, Inc. is registered with the FDA (registration 3010552191) in Milpitas, CA, United States. It lists 7 device types. The FDA files 4 510(k) clearances under its listings, the newest dated July 9, 2026. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3010552191
- FEI number
- 3015191855
- Address
- 426 South Hillview Drive, Milpitas, CA, United States, 95035
- Owner or operator
- LifeSignals, Inc (10045399)
- Roles
- Complaint file establishment, Specification developer
- First device listed
- August 1, 2020
- Registered through
- 2026
- Brand names listed
- LifeSignals, UbiqVue, UbiqVue 2A Multiparameter System
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Continuous Measurement Thermometer | FLL | 2 | Complaint file establishment, Specification developer | accessdata.fda.gov |
| Electrocardiograph, Ambulatory (Without Analysis) | MWJ | 2 | Complaint file establishment, Specification developer | accessdata.fda.gov |
| Monitor, Physiological, Patient(With Arrhythmia Detection Or Alarms) | MHX | 2 | Complaint file establishment, Specification developer | accessdata.fda.gov |
| Outpatient Cardiac Telemetry | QYX | 2 | Complaint file establishment, Specification developer | accessdata.fda.gov |
| Oximeter | DQA | 2 | Complaint file establishment, Specification developer | accessdata.fda.gov |
| Transmitters And Receivers, Electrocardiograph, Telephone | DXH | 2 | Complaint file establishment, Specification developer | accessdata.fda.gov |
| Transmitters And Receivers, Physiological Signal, Radiofrequency | DRG | 2 | Complaint file establishment, Specification developer | accessdata.fda.gov |
510(k) clearances
The 510(k) numbers this establishment lists, with the FDA decision on each. The applicant is the company that holds the clearance.
| Decided | 510(k) number | Device | Product code | Decision | Applicant | Source |
|---|---|---|---|---|---|---|
| July 9, 2026 | K261569 | UbiqVue 2AYe Cardiac System (UX2253) | DRG | Substantially Equivalent | Lifesignals, Inc. | accessdata.fda.gov |
| November 12, 2024 | K242018 | UbiqVue 2A Multi-parameter System (UX2550) | DRG | Substantially Equivalent | Lifesignals, Inc. | accessdata.fda.gov |
| July 21, 2021 | K202868 | LifeSignals Multi-Parameter Remote Monitoring Platform | DRG | Substantially Equivalent | Lifesignals, Inc. | accessdata.fda.gov |
| July 15, 2020 | K200690 | LifeSignals ECG Remote Monitoring Patch Platform | DRG | Substantially Equivalent | Lifesignals, Inc. | accessdata.fda.gov |
Compare with other makers
- All makers of Transmitters And Receivers, Physiological Signal, Radiofrequency
- All makers of Electrocardiograph, Ambulatory (Without Analysis)
- All makers of Monitor, Physiological, Patient(With Arrhythmia Detection Or Alarms)
- All makers of Oximeter
- All makers of Continuous Measurement Thermometer
- All makers of Transmitters And Receivers, Electrocardiograph, Telephone
Updated July 9, 2026. Read from openFDA bulk downloads (device registration and listing, 510(k), PMA, recall and enforcement files). CC0 1.0, public domain (openFDA terms of service). The files are joined on FDA identifiers: the 510(k) and PMA numbers a registration lists, and the recalling firm's FEI for recalls. Recall class comes from the FDA enforcement report. The FDA states that openFDA data is unvalidated and is not for decisions about medical care. Free to reuse with credit to SpecStream under CC BY 4.0. Spot a wrong value? Write to [email protected] with the link to this page.