Medical Device Manufacturer · US , Chatham , NJ

Lone Star Technologies - FDA 510(k) Cleared Devices

2 submissions · 2 cleared · Since 1998
2
Total
2
Cleared
0
Denied

Lone Star Technologies has 2 FDA 510(k) cleared medical devices. Based in Chatham, US.

Historical record: 2 cleared submissions from 1998 to 1998. Primary specialty: Dental.

Browse the FDA 510(k) cleared devices submitted by Lone Star Technologies Filter by specialty or product code using the sidebar.

FDA 510(k) Regulatory Record - Lone Star Technologies

2 devices
1-2 of 2
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