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.
Catalogue
Search and filter all 1,530 devicesShowing 1-50 of 1,530
Company details
- FDA FEI number
- 1000403400
- Address
- 11705 Nw 39th St, Coral Springs, FL, 33065
FDA recalls
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.
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.
- 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
Frequently asked questions
How many devices does LifeSync Corporation have in the registry?
The registry currently lists 1530 devices for LifeSync Corporation. Devices recorded under merged duplicate company entries are counted once.
Which registries list LifeSync Corporation's devices?
Among its 50 most recently registered devices, LifeSync Corporation has devices listed in FDA GUDID (50 devices).
What risk classes do LifeSync Corporation's devices fall under?
Among its 50 most recently registered devices, the classes recorded for LifeSync Corporation's devices are Class II. Each device page shows its own class and authorisation.
Are there FDA recall records for LifeSync Corporation?
FDA recall records list 2 recalls initiated by LifeSync Corporation, the most recent initiated on 2007-12-13. A recall is often a precaution started by the manufacturer; the records say nothing about the company's overall record.
What are the newest devices from LifeSync Corporation in the registry?
The most recently registered devices listed for LifeSync Corporation include AMC RPO-LW-329DS120/5A, AMC RPO-LW-329DS50/5A, AMC YM-513DIN and AMC YM-515DIN.