Founded in 1986, Syntron manufactures rapid in vitro diagnostic tests and detection readers. We are licensed as a Medical Device Establishment by the US FDA and the State of California Department of Health Services. Syntron is an ISO certified company. Many of our products are 510(k) cleared, CLIA waived, CE and OTC. Some products are for physician offices and home use.
Professional Tests
Clinics
Hospitals
Re-habitation Centers
Employee Screening
Point of Care
CLIA Waived
CE Marked
OEM & CMO
Product production
Product assembly
Product formulation
Over the Counter Tests
Private Label
Value Brand
Major Brand