Medical Device Manufacturer · IL , Binyamina

Light Instrument, Ltd. - FDA 510(k) Cleared Devices

1 submissions · 1 cleared · Since 2006
1
Total
1
Cleared
0
Denied

Light Instrument, Ltd. has 1 FDA 510(k) cleared medical devices. Based in Binyamina, IL.

Historical record: 1 cleared submissions from 2006 to 2006. Primary specialty: General & Plastic Surgery.

Browse the FDA 510(k) cleared devices submitted by Light Instrument, Ltd. Filter by specialty or product code using the sidebar.

FDA 510(k) Regulatory Record - Light Instrument, Ltd.

1 devices
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