FDA device listing
ALIF Hive-A Interbody Spacer,Hive AL Interbody System,Hive O-AL Interbody System,Hive PL Interbody System,Hive TL…
FDA device listing 1873815123 · NanoHive Medical
Key facts
| Proprietary names | ALIF Hive-A Interbody Spacer,Hive AL Interbody System,Hive O-AL Interbody System,Hive PL Interbody System,Hive TL Interbody System,NanoHive Medical Lumbar Interbody System,PLIF Hive-P Interbody Spacer,TLIF Hive-T Curved Interbody Spacer,TLIF Hive-T Interbody Spacer |
|---|---|
| Owner/operator | NanoHive Medical |
| Owner/operator number | 10055679 |
| Premarket submissions | K170676 |
| Product codes | MAX |
| Device names | MAX - Intervertebral Fusion Device With Bone Graft, Lumbar |
| Device class | Class II |
| Classification regulations (21 CFR) | 888.3080 |
| Review panels | Orthopedic |
| Registered establishments | NanoHive Medical LLC |
| Establishment registrations | 3013462427 |
| FEI numbers | 3013462427 |
| Establishment operations | Manufacturer, Specification Developer |
| Registration valid through | 2026 |
At a glance
- 1–9 Registered establishments listing this device
- 100–999 UDI devices (GUDID) under the same submission
- 1–9 Device listings citing the same submission
- Yes Premarket submission listed
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About FDA device listings
Establishments that make or process devices for the U.S. market must list each device with the FDA. A listing records the device's proprietary names, product codes and premarket submission, and every registered establishment that handles it.
Source: U.S. Food and Drug Administration (FDA), Establishment Registration and Device Listing database