Neurodynamics, Inc.
Country not established FDA establishment FEI 2434444
- Devices
- 4
- Registrations
- FDA
- FDA recalls
- 0
Catalogue
Modification To Ghajar Guide Twist Drill Ref K932402
510(k) 510(k)Tri-Flow Catheter Ref K875205
510(k) 510(k)Ghajar Guide System For The Perforator Ref K875019
510(k) 510(k)Ghajar Guide Twist Drill Ref K875018
510(k) 510(k)
Company details
- FDA FEI number
- 2434444
- Address
- 340 East 93 Street, Manhattan, NY, 10128
Frequently asked questions
How many devices does NEURODYNAMICS, INC. have in the registry?
The registry currently lists 4 devices for NEURODYNAMICS, INC.. Devices recorded under merged duplicate company entries are counted once.
Which registries list NEURODYNAMICS, INC.'s devices?
Among its 4 most recently registered devices, NEURODYNAMICS, INC. has devices listed in FDA 510(k) (4 devices).
What risk classes do NEURODYNAMICS, INC.'s devices fall under?
Among its 4 most recently registered devices, the classes recorded for NEURODYNAMICS, INC.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from NEURODYNAMICS, INC. in the registry?
The most recently registered devices listed for NEURODYNAMICS, INC. include MODIFICATION TO GHAJAR GUIDE TWIST DRILL, TRI-FLOW CATHETER, GHAJAR GUIDE SYSTEM FOR THE PERFORATOR and GHAJAR GUIDE TWIST DRILL.