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Idys®-LLIF 3DTi

FDA UDI

Class II (US FDA UDI)

by Clariance, Inc.

Identity

Trade Name
Idys®-LLIF 3DTi FDA UDI
Generic Name
Metallic spinal interbody fusion cage FDA UDI
Device Name
LLIF 3DTi Plate FDA UDI
Model / Reference
51430007-S FDA UDI
Description
LLIF 3DTi Plate FDA UDI

Identifiers

Catalog Number
51430007-S FDA UDI
Primary DI / UDI-DI
03700780634491 FDA UDI
510(k) Number
K202032 FDA UDI
FDA Product Code
OVD FDA UDI
GMDN Term
Metallic spinal interbody fusion cage 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

Yes

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 — 7 Millimeter FDA UDI

Category: Metallic spinal interbody fusion cage

Idys®-LLIF 3DTi by Clariance, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Metallic spinal interbody fusion cage.

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 570e2609-d127-4ee4-b598-b2f39c21a979 37 fields · synced May 30, 2026