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LifeSync Corporation

Country not established FDA establishment FEI 1000403400

Devices
1,530
Registrations
FDA
FDA recalls
2

What LifeSync Corporation makes

LifeSync Corporation manufactures medical device adapters, including the LS-302 model, designed for connecting or interfacing with medical equipment to ensure compatibility and functionality.

The company’s products are classified as Class II devices under FDA regulations and are listed via the 510(k) pathway. The portfolio is regulated in the United States.

AI-generated from registry data, 26 Oct 2026. Not verified by deviCERTS or the manufacturer.

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Company details

FDA FEI number
1000403400
Address
11705 Nw 39th St, Coral Springs, FL, 33065

FDA recalls2

Recalls are matched to the firm by name. FDA recall data as of 22 Oct 2026.

FDA recall records list 2 recalls initiated by LifeSync Corporation, initiated on 2007-12-13. By recorded status: 2 terminated. The reasons filed fall into these groups: other reasons as filed. A recall is often a precaution started by the manufacturer, and a count of records is not a verdict on a company.

Generated automatically from FDA recall records, as a summary of the records listed below. It describes what the records state and is not an assessment of this manufacturer.

  • 2007

    • 13 Dec 2007 Z-1659-2008 Unclassified (pre-2012) Terminated LifeSync Wireless ECG System - Intermittent failure when using LS-202 and LS-232 LeadWear in conjunction with LS-41245 and LS-41285 Adaptors. The out of box failure manifests as a V-Lead failure, leading to a possible delay in treatment based upon a delay in ECG monitoring. Distribution: Class II Recall - Nationwide Distribution. Submission number: K030795
    • 13 Dec 2007 Z-1660-2008 Unclassified (pre-2012) Terminated LifeSync Wireless ECG System - Intermittent failure when using LS-202 and LS-232 LeadWear in conjunction with LS-41245 and LS-41285 Adaptors. The out of box failure manifests as a V-Lead failure, intended for use as a radiofrequency signal transmitter and receiver of electrocardiograph physiological signals which are displayed on the ECG monitors of various manufacturers' systems that have been Distribution: Class II Recall - Nationwide Distribution. Submission number: K030795

This is an FDA establishment record. No EUDAMED registration is known for this company.