ENZA™-A Titanium ALIF

FDA UDI

Class II (US FDA UDI)

by Camber Spine Technologies

Identity

Trade Name: ENZA™-A Titanium ALIF FDA UDI
Generic Name: Metallic spinal fusion cage, non-sterile FDA UDI
Device Name: Bi-Convex 8° Lordotic, 26mm x 32mm, 15mm FDA UDI
Model / Reference: EZAT-2632-0815 FDA UDI
Description: Bi-Convex 8° Lordotic, 26mm x 32mm, 15mm FDA UDI

Identifiers

Primary DI / UDI-DI: B030EZAT263208150 FDA UDI
510(k) Number: K153720 FDA UDI
K173432 FDA UDI
FDA Product Code: OVD 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

Yes

FDA UDI

Sterilization Method

Moist Heat or Steam Sterilization FDA UDI

Dimensions & Sizes

Size: Depth — 26 Millimeter FDA UDI
Width — 32 Millimeter FDA UDI
Height — 15 Millimeter FDA UDI

Category: Metallic spinal fusion cage, non-sterile

ENZA™-A Titanium ALIF by Camber Spine Technologies — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

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

Silverstone Titanium Interbody Fusion System — Altus Spine · Class II
Silverstone Titanium Interbody Fusion System — Altus Spine · Class II
TraXis® — ZIMMER SPINE, INC. · Class II
PLIF Cage — Eisertech, LLC · Class II
IVA Cage Ti — Dio Medical Co., Ltd. · Class II
Copperhead — EMINENT SPINE LLC · Class II
IVA Cage Ti — Dio Medical Co., Ltd. · Class II
3DP Lumbar Interbody System — Genesys Orthopedics Systems LLC · Class II

Cleared under the same submission

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: Camber Spine Technologies

Sources (1)

FDA UDI 9087508f-7239-45f5-9d21-1875a69dacc7 36 fields · synced Jun 1, 2026