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FOCUS Interbody System

FDA UDI

Class II (US FDA UDI)

by OrthoCircle Spine

Identity

Trade Name
FOCUS Interbody System FDA UDI
Generic Name
Metallic spinal interbody fusion cage FDA UDI
Device Name
27L x 10W x 10H x 5 LA FDA UDI
Model / Reference
203.2110 FDA UDI
Description
27L x 10W x 10H x 5 LA FDA UDI

Identifiers

Primary DI / UDI-DI
00810005112468 FDA UDI
FDA Product Code
MAX 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

No

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

Category: Metallic spinal interbody fusion cage

FOCUS Interbody System by OrthoCircle Spine — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Metallic spinal interbody fusion cage.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
OrthoCircle Spine

Sources (1)

  • FDA UDI aa1efd5f-d07b-48fc-a49a-5b90440dd4e9 33 fields · synced Jun 6, 2026