Lineum Oct Spine System

FDA UDI

Class II (US FDA UDI)

by Biomet Spine Llc

Identity

Trade Name: LINEUM OCT SPINE SYSTEM FDA UDI
Generic Name: Surgical screwdriver, reusable FDA UDI
Model / Reference: 14-525051 FDA UDI

Identifiers

Catalog Number: 14-525051 FDA UDI
Primary DI / UDI-DI: 00888480511533 FDA UDI
FDA Product Code: MNH FDA UDI
KWP FDA UDI
MNI FDA UDI
MQP FDA UDI
MAX FDA UDI
GMDN Term: Surgical screwdriver, reusable FDA UDI

Classification

Device Class: Class II FDA UDI
Regulation Number: 888.3070 FDA UDI
888.3050 FDA UDI
888.3060 FDA UDI
888.3080 FDA UDI
Commercial Distribution: In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

FDA UDI

Single Use

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

Category: Surgical screwdriver, reusable

Lineum Oct Spine System by Biomet Spine Llc — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

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LOSPA IS Spinal Fixation System — Corentec Co., Ltd · Class II
PERLA ® TL — Spineart · Class II
USS — Synthes · Class I
Whistler Modular Pedicle Screw System — EVOLUTION SPINE, LLC · Class I
CosmoLock Pedicle Screw System — Kalitec Direct LLC · Class I

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: Biomet Spine Llc

Sources (1)

FDA UDI 695d2827-6e34-4bac-ba48-62fb18421ae5 35 fields · synced May 30, 2026