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Idys™- ALIF

FDA UDI

Class II (US FDA UDI)

by Clariance, Inc.

Identity

Trade Name
Idys™- ALIF FDA UDI
Generic Name
Polymeric spinal fusion cage, sterile FDA UDI
Device Name
ALIF CAGE FDA UDI
Model / Reference
24520418-S FDA UDI
Description
ALIF CAGE FDA UDI

Identifiers

Catalog Number
24520418-S FDA UDI
Primary DI / UDI-DI
03700780626939 FDA UDI
510(k) Number
K172083 FDA UDI
FDA Product Code
OVD 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

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Dimensions & Sizes

Size
Height — 1418 Millimeter FDA UDI
Depth — 26 Millimeter FDA UDI
Width — 32 Millimeter FDA UDI

Category: Polymeric spinal fusion cage, sterile

Idys™- ALIF by Clariance, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Polymeric spinal fusion cage, sterile.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Clariance, Inc.

Sources (1)

  • FDA UDI 9b1dfe7b-7c2f-4e70-b3db-19de58a62cd7 37 fields · synced May 30, 2026