InFix®

FDA UDI

Class II (US FDA UDI)

by Zimmer Spine, Inc.

Identity

Trade Name: InFix® FDA UDI
Generic Name: Metallic spinal fusion cage, non-sterile FDA UDI
Model / Reference: 1803-12 FDA UDI

Identifiers

Catalog Number: 1803-12 FDA UDI
Primary DI / UDI-DI: 00889024331174 FDA UDI
FDA Product Code: MAX FDA UDI
MQP 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
888.3060 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

Dimensions & Sizes

Size: Width — 12 Millimeter FDA UDI

Category: Metallic spinal fusion cage, non-sterile

InFix® by Zimmer Spine, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

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

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PLIF Cage — Eisertech, LLC · Class II
IVA Cage Ti — Dio Medical Co., Ltd. · Class II
Copperhead — EMINENT SPINE LLC · Class II
SPIRA™-C Open Matrix Cervical Interbody — CAMBER SPINE TECHNOLOGIES · Class II
IVA Cage Ti — Dio Medical Co., Ltd. · Class II
3DP Lumbar Interbody System — Genesys Orthopedics Systems LLC · 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: Zimmer Spine, Inc.

Sources (1)

FDA UDI 0a4d50ec-9e12-4193-8c68-9c23597e0081 35 fields · synced May 30, 2026