JULIET ® Ti OL

FDA UDI

Class II (US FDA UDI)

by Spineart

Identity

Trade Name: JULIET ® Ti OL FDA UDI
Generic Name: Metallic spinal interbody fusion cage FDA UDI
Device Name: LUMBAR POSTERIOR Ti CAGE FDA UDI
Model / Reference: JUT-O6 32 16-S FDA UDI
Description: LUMBAR POSTERIOR Ti CAGE FDA UDI

Identifiers

Catalog Number: JUT-O6 32 16-S FDA UDI
Primary DI / UDI-DI: 07640178973312 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

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

FDA UDI

Convenience Kit

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

Yes

FDA UDI

Dimensions & Sizes

Size: Angle — 6 degree FDA UDI
Length — 32 Millimeter FDA UDI
Width — 10.5 Millimeter FDA UDI
Height — 16 Millimeter FDA UDI

Category: Metallic spinal interbody fusion cage

A comprehensive medical device directory entry for the JULIET Ti OL, an intervertebral fusion device with bone graft. This device is designed to provide mechanical stability and sufficient space for therapeutic spinal bone fusion to occur, typically in the treatment of degenerative disc disease.

Similar devices

Also classified as Metallic spinal interbody fusion cage.

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Peridot-PT Anterior Cervical Intervertebral body fusion system — GBS Commonwealth Co., Ltd. · Class II
CoRoent — Nuvasive, Inc. · Class II
Kyocera Medical Technologies, Inc. — Kyocera Medical Technologies, Inc. · Class II
MectaLIF 3D — Medacta International · Class II
PILLAR TL — Orthofix US LLC · Class II
Solar™ Interbody Fusion System — Degen Medical · Class II
Peridot-TD Anterior Cervical Intervertebral body fusion system — GBS Commonwealth Co., Ltd. · Class II

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: Spineart

Sources (1)

FDA UDI 0e154edc-ffc3-4844-8390-df067526fe9a 35 fields · synced Jul 25, 2026