Marizyme
Also registered as Marizyme, Inc.
United Statesfrom the FDA registration address FDA FEI 3011421726
- Devices
- 2
- Registrations
- FDA
- FDA recalls
- 0
At a glance
Market reach
- United States
- FDA FEI
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
DuraGraft Ref DEN230002
Regimes: De Novo Registry: De NovoDuraGraft Vascular Conduit Solution Ref K240925
Regimes: 510(k) Registry: 510(k)
Company details
- FDA FEI number
- 3011421726
- Address
- 1645 Palm Beach Lakes Blvd Ste 1200, West Palm Bch, FL, 33401
Frequently asked questions
How many devices does Marizyme have in the registry?
The registry currently lists 2 devices for Marizyme. Devices recorded under merged duplicate company entries are counted once.
Which registries list Marizyme's devices?
Among its 2 most recently registered devices, Marizyme has devices listed in FDA 510(k) (2 devices).
What risk classes do Marizyme's devices fall under?
Among its 2 most recently registered devices, the classes recorded for Marizyme's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Marizyme in the registry?
The most recently registered devices listed for Marizyme include DuraGraft and DuraGraft Vascular Conduit Solution.