Neurodelivery Technology, Inc.
United StatesFDA applicant, unverified
- Devices
- 3
What Neurodelivery Technology, Inc. makes
Neurodelivery Technology, Inc. produces sterile, single-use trays for epidural and spinal anesthesia procedures, including combined epidural-spinal trays and custom spinal/epidural sets. These trays are designed for use in surgical and procedural settings to administer local anesthesia via epidural or spinal routes.
The company’s products are classified as Class II medical devices under FDA regulations and are supported by 510(k) clearances. The devices are listed in the FDA’s 510(k) database and are manufactured in the United States.
Catalogue
E-Sp Combined Epidural-Spinal Anesthesia Tray Ref K933711
Regimes: 510(k) Registry: 510(k)Epidural Anesthesia Procedure Tray, Custom Ref K933721
Regimes: 510(k) Registry: 510(k)Micro-Sp Custom Spinal Anesthesia Tray Ref K934526
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Neurodelivery Technology, Inc. have in the registry?
The registry currently lists 3 devices for Neurodelivery Technology, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Neurodelivery Technology, Inc.'s devices?
Among its 3 most recently registered devices, Neurodelivery Technology, Inc. has devices listed in FDA 510(k) (3 devices).
What risk classes do Neurodelivery Technology, Inc.'s devices fall under?
Among its 3 most recently registered devices, the classes recorded for Neurodelivery Technology, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Neurodelivery Technology, Inc. in the registry?
The most recently registered devices listed for Neurodelivery Technology, Inc. include E-SP COMBINED EPIDURAL-SPINAL ANESTHESIA TRAY, EPIDURAL ANESTHESIA PROCEDURE TRAY, CUSTOM and MICRO-SP CUSTOM SPINAL ANESTHESIA TRAY.