Medical Device Manufacturer · IL , Nazareth

Endogi Medical, Ltd. - FDA 510(k) Cleared Devices

2 submissions · 1 cleared · Since 2020
2
Total
1
Cleared
0
Denied

Endogi Medical, Ltd. has 1 FDA 510(k) cleared medical devices. Based in Nazareth, IL.

Last cleared in 2023. Active since 2020. Primary specialty: Gastroenterology & Urology.

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

510(k) submissions have been managed by ProMedoss, Inc. as regulatory consultant.

FDA 510(k) Regulatory Record - Endogi Medical, Ltd.
2 devices
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