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Ngage

FDA UDI

Class II (US FDA UDI)

by Orthofix US LLC

Identity

Trade Name
NGAGE FDA UDI
Generic Name
Metallic spinal interbody fusion cage FDA UDI
Device Name
NGAGE 4-LOBE 14MM MESH, 30MM FDA UDI
Model / Reference
74-1430 FDA UDI
Description
NGAGE 4-LOBE 14MM MESH, 30MM FDA UDI

Identifiers

Primary DI / UDI-DI
18257200073337 FDA UDI
510(k) Number
K032700 FDA UDI
FDA Product Code
MQP FDA UDI
GMDN Term
Metallic spinal interbody fusion cage FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
888.3060 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

No

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

No

FDA UDI

Manufacturing Date

No

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Metallic spinal interbody fusion cage

Ngage by Orthofix US 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

Manufacturer
Orthofix US LLC

Sources (1)

  • FDA UDI e7bc3e6e-d9c7-446e-8a25-68808ad52a0c 35 fields · synced Jun 8, 2026