← Back to catalogue

NanoHive IBFD

FDA UDI

Class II (US FDA UDI)

by NanoHive Medical LLC

Identity

Trade Name
NanoHive IBFD FDA UDI
Generic Name
Metallic spinal interbody fusion cage FDA UDI
Device Name
TLIF, 09W, 26L, 12H, 8° FDA UDI
Model / Reference
03-A-0005-4012 FDA UDI
Description
TLIF, 09W, 26L, 12H, 8° FDA UDI

Identifiers

Primary DI / UDI-DI
00817493021029 FDA UDI
510(k) Number
K170676 FDA UDI
FDA Product Code
MAX 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

No

FDA UDI

Dimensions & Sizes

Size
Angle — 8 degree FDA UDI
Width — 9 Millimeter FDA UDI
Length — 26 Millimeter FDA UDI
Height — 12 Millimeter FDA UDI

Category: Metallic spinal interbody fusion cage

NanoHive IBFD 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

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Sources (1)

  • FDA UDI d61bbbe6-0d6e-405a-80db-0aee630ac9a4 36 fields · synced Jun 1, 2026