Medical Device Manufacturer · US , Bethesda , MD

Celestray Biotech Company, LLC.,

2 submissions · 2 cleared · Since 2023
2
Total
2
Cleared
0
Denied

Celestray Biotech Company, LLC., — FDA 510(k) Submissions

Celestray Biotech Company, LLC., has submitted 2 FDA 510(k) premarket notifications since 2023, of which 2 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Mesh, Surgical, Absorbable, Orthopaedics, Reinforcement Of Tendon, Cuff, Nerve . Use the specialty filter in the sidebar to narrow results.

2 devices
1–2 of 2
Filters
Filter by Specialty
All2 Orthopedic 1 Neurology 1