SpaceVision® OLIF

FDA UDI

Class II (US FDA UDI)

by Spine Vision, Inc.

Identity

Trade Name: SpaceVision® OLIF FDA UDI
Generic Name: Polymeric spinal fusion cage, sterile FDA UDI
Device Name: Sterile OLIF cage H07-L32 FDA UDI
Model / Reference: SPL1-OC07-32 FDA UDI
Description: Sterile OLIF cage H07-L32 FDA UDI

Identifiers

Primary DI / UDI-DI: 03663136030456 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

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

Dimensions & Sizes

Size: Length — 32 Millimeter FDA UDI
Height — 07 Millimeter FDA UDI

Category: Polymeric spinal fusion cage, sterile

SpaceVision® OLIF by Spine Vision, 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: Spine Vision, Inc.

Sources (1)

FDA UDI f60d3077-7033-4649-94cb-29e00b9e4172 35 fields · synced Jun 8, 2026