Luna 3D

FDA UDI

Class II (US FDA UDI)

by Benvenue Medical, Inc.

Identity

Trade Name: Luna 3D FDA UDI
Generic Name: Polymeric spinal fusion cage, sterile FDA UDI
Device Name: 13mm, 8-Degree, Luna 3D Lordotic Implant Kit FDA UDI
Model / Reference: LUN3013-08 FDA UDI
Description: 13mm, 8-Degree, Luna 3D Lordotic Implant Kit FDA UDI

Identifiers

Catalog Number: LUN3013-08 FDA UDI
Primary DI / UDI-DI: 00813478020346 FDA UDI
FDA Product Code: MAX FDA UDI
GMDN Term: Polymeric spinal fusion cage, sterile 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

FDA UDI

Contains Latex

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

FDA UDI

Convenience Kit

Yes

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

FDA UDI

MRI Safety

MR Conditional FDA UDI

Category: Polymeric spinal fusion cage, sterile

Luna 3D by Benvenue Medical, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

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Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Source	Region	Type	Cert / Approval No.	Class	Status
FDA UDI	United States	FDA UDI	Registered in GUDID	Class II	Pending data

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Manufacturer

Manufacturer: Benvenue Medical, Inc.

Sources (1)

FDA UDI 6d0ab3a8-ddcc-4254-b565-ce8ec40c1d1e 35 fields · synced May 29, 2026