Fesarius Therapeutics
Also registered as Fesariustherapeutics, Inc.
Country not established FDA establishment FEI 3036710971
- Devices
- 3
- Registrations
- FDA
- FDA recalls
- 0
Catalogue
- GUDID
- GUDID
DermiSphere Dermal Template Ref K241904
510(k) 510(k)
Company details
- FDA FEI number
- 3036710971
- Address
- 619 W 54th St, New York, NY, 10019
Frequently asked questions
How many devices does FESARIUS THERAPEUTICS have in the registry?
The registry currently lists 3 devices for FESARIUS THERAPEUTICS. Devices recorded under merged duplicate company entries are counted once.
Which registries list FESARIUS THERAPEUTICS's devices?
Among its 3 most recently registered devices, FESARIUS THERAPEUTICS has devices listed in FDA 510(k) (1 device) and FDA GUDID (2 devices). A device can be listed in more than one registry, so these counts overlap.
What are the newest devices from FESARIUS THERAPEUTICS in the registry?
The most recently registered devices listed for FESARIUS THERAPEUTICS include DermiSphere™ hDRT DermiSphere Dermal Template and DermiSphere Dermal Template.