Celestray Biotech Company, LLC.,
United StatesFDA applicant, unverified FDA FEI 3027699572
- Devices
- 2
- Registrations
- FDA
- FDA recalls
- 0
At a glance
Market reach
- United States
- FDA FEI
What Celestray Biotech Company, LLC., makes
Celestray Biotech Company, LLC produces absorbable fibrous membranes and nerve guidance conduits designed for surgical applications, including tissue integration and peripheral nerve repair.
These devices are classified as Class II under FDA regulations and are authorised via the 510(k) pathway. The company is based in the United States.
Catalogue
SpinMedix Absorbable Fibrous Membrane Ref K222220
Regimes: 510(k) Registry: 510(k)Rebuilder Nerve Guidance Conduit Ref K230794
Regimes: 510(k) Registry: 510(k)
Company details
- FDA FEI number
- 3027699572
- Address
- 8712 Irvington Ave, Bethesda, MD, 20827
Frequently asked questions
How many devices does Celestray Biotech Company, LLC., have in the registry?
The registry currently lists 2 devices for Celestray Biotech Company, LLC.,. Devices recorded under merged duplicate company entries are counted once.
Which registries list Celestray Biotech Company, LLC.,'s devices?
Among its 2 most recently registered devices, Celestray Biotech Company, LLC., has devices listed in FDA 510(k) (2 devices).
What risk classes do Celestray Biotech Company, LLC.,'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for Celestray Biotech Company, LLC.,'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Celestray Biotech Company, LLC., in the registry?
The most recently registered devices listed for Celestray Biotech Company, LLC., include SpinMedix Absorbable Fibrous Membrane and Rebuilder Nerve Guidance Conduit.