Irix-A Lumbar Integrated Fusion System

FDA UDI

Class II (US FDA UDI)

by Xtant Medical Holdings, Inc.

Identity

Trade Name: Irix-A Lumbar Integrated Fusion System FDA UDI
Generic Name: Spinal bone screw, non-bioabsorbable FDA UDI
Device Name: 5.5 X 40mm, IRIX-A, SELF DRILLING SCREW FDA UDI
Model / Reference: X080-5540SDX FDA UDI
Description: 5.5 X 40mm, IRIX-A, SELF DRILLING SCREW FDA UDI

Identifiers

Primary DI / UDI-DI: M697X0805540SDX1 FDA UDI
FDA Product Code: OVD FDA UDI
GMDN Term: Spinal bone screw, 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

FDA UDI

Single Use

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

FDA UDI

Manufacturing Date

FDA UDI

Sterilization Method

Moist Heat or Steam Sterilization FDA UDI

Dimensions & Sizes

Size: Length — 40 Millimeter FDA UDI
Outer Diameter — 5.5 Millimeter FDA UDI

Category: Spinal bone screw, non-bioabsorbable

Irix-A Lumbar Integrated Fusion System by Xtant Medical Holdings, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

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Also classified as Spinal bone screw, non-bioabsorbable.

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AccelFix Spinal Fixation System (Sterile) — L&K Biomed · Class IIb
Proficient™ Posterior Cervical Spine System — Spine Wave, 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: Xtant Medical Holdings, Inc.

Sources (1)

FDA UDI b67ae794-fb91-4e22-bba2-b3b6f38b37e5 35 fields · synced Jun 1, 2026