Intelis Instruments , Ltd. - FDA 510(k) Cleared Devices
1
Total
1
Cleared
0
Denied
Intelis Instruments , Ltd. has 1 FDA 510(k) cleared medical devices. Based in Hadera, IL.
Last cleared in 2021. Active since 2021. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Intelis Instruments , Ltd. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by A. Stein - Regulatory Affairs Consulting , Ltd. as regulatory consultant.
1 devices