JULIET ® Ti LL

FDA UDI

Class II (US FDA UDI)

by Spineart

Identity

Trade Name: JULIET ® Ti LL FDA UDI
Generic Name: Spinal fixation plate, non-bioabsorbable FDA UDI
Device Name: LATERAL LUMBAR TI-LIFE PLATE LARGE FDA UDI
Model / Reference: JLT-PL 04 18-S FDA UDI
Description: LATERAL LUMBAR TI-LIFE PLATE LARGE FDA UDI

Identifiers

Catalog Number: JLT-PL 04 18-S FDA UDI
Primary DI / UDI-DI: 07640178987500 FDA UDI
FDA Product Code: OVD FDA UDI
MAX FDA UDI
GMDN Term: Spinal fixation plate, non-bioabsorbable 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

MRI Safety

MR Conditional FDA UDI

Dimensions & Sizes

Size: Height — 18 Millimeter FDA UDI

Category: Spinal fixation plate, non-bioabsorbable

JULIET ® Ti LL by Spineart — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Spinal fixation plate, non-bioabsorbable.

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PROVIDENCE — GLOBUS MEDICAL, INC. · Class II
ACP — Nuvasive, Inc. · Class II
uNion Cervical Plate System — ULRICH MEDICAL USA, INC. · 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 aa816eba-cd37-46ed-85e8-35b1484e7884 35 fields · synced May 30, 2026