Medical Device Manufacturer · US , Jupiter , FL

Marizyme - FDA 510(k) Cleared Devices

1 submissions · 1 cleared · Since 2024
1
Total
1
Cleared
0
Denied

Marizyme has 1 FDA 510(k) cleared medical devices. Based in Jupiter, US.

Latest FDA clearance: May 2024. Active since 2024. Primary specialty: Gastroenterology & Urology.

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

510(k) submissions have been managed by Hogan Lovells US LLP as regulatory consultant.

FDA 510(k) Regulatory Record - Marizyme
1 devices
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