Opticage Expandable Interbody Implant

FDA UDI

Class II (US FDA UDI)

by Interventional Spine, Inc

Identity

Trade Name: Opticage Expandable Interbody Implant FDA UDI
Generic Name: Metallic spinal fusion cage, non-sterile FDA UDI
Device Name: 11mm Width x 21mm Length by 9mm-14mm Expandable Height FDA UDI
Model / Reference: 9070-06 FDA UDI
Description: 11mm Width x 21mm Length by 9mm-14mm Expandable Height FDA UDI

Identifiers

Catalog Number: 9070-06 FDA UDI
Primary DI / UDI-DI: 81195401101786 FDA UDI
FDA Product Code: MAX FDA UDI
GMDN Term: Metallic spinal fusion cage, non-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

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

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

FDA UDI

Manufacturing Date

FDA UDI

Sterilization Method

Moist Heat or Steam Sterilization FDA UDI

MRI Safety

MR Safe FDA UDI

Category: Metallic spinal fusion cage, non-sterile

Opticage Expandable Interbody Implant by Interventional Spine, Inc — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

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Also classified as Metallic spinal fusion cage, non-sterile.

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SPIRA™-C Open Matrix Cervical Interbody — CAMBER SPINE TECHNOLOGIES · Class II
IVA Cage Ti — Dio Medical 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: Interventional Spine, Inc

Sources (1)

FDA UDI 8b052318-fb7a-4586-8f3f-09a826b6a92a 35 fields · synced Jun 1, 2026