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Hive™ Standalone ALIF System

FDA UDI

Class II (US FDA UDI)

by NanoHive Medical LLC

Identity

Trade Name
Hive™ Standalone ALIF System FDA UDI
Generic Name
Metallic spinal interbody fusion cage FDA UDI
Device Name
42W x 28L, 19H, 8° - Jar Package Configuration FDA UDI
Model / Reference
06-A-0025-4019 FDA UDI
Description
42W x 28L, 19H, 8° - Jar Package Configuration FDA UDI

Identifiers

Primary DI / UDI-DI
00817493027366 FDA UDI
510(k) Number
K200541 FDA UDI
FDA Product Code
MAX FDA UDI
OVD FDA UDI
GMDN Term
Metallic spinal interbody fusion cage FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
888.3080 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

FDA UDI

Implantable

Yes

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Dimensions & Sizes

Size
Width — 42 Millimeter FDA UDI
Length — 28 Millimeter FDA UDI
Angle — 8 degree FDA UDI
Height — 19 Millimeter FDA UDI

Category: Metallic spinal interbody fusion cage

Hive™ Standalone ALIF System by NanoHive Medical LLC — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Metallic spinal interbody fusion cage.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI a09cdbd7-d48c-4596-a9d6-e112246bb37c 36 fields · synced May 30, 2026