← Back to catalogue

Coalition

FDA UDI

Class I (US FDA UDI)

by Globus Medical, Inc.

Identity

Trade Name
COALITION FDA UDI
Generic Name
General internal orthopaedic fixation system implantation kit FDA UDI
Device Name
Midline Holding Tip, 10mm FDA UDI
Model / Reference
6128.4010 FDA UDI
Description
Midline Holding Tip, 10mm FDA UDI

Identifiers

Primary DI / UDI-DI
00889095175479 FDA UDI
510(k) Number
K142218 FDA UDI
FDA Product Code
LXH FDA UDI
GMDN Term
General internal orthopaedic fixation system implantation kit FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
888.4540 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

No

FDA UDI

Implantable

No

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

No

FDA UDI

Manufacturing Date

No

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Dimensions & Sizes

Size
Height — 10 Millimeter FDA UDI

Category: General internal orthopaedic fixation system implantation kit

Coalition by Globus Medical, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as General internal orthopaedic fixation system implantation kit.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Sources (1)

  • FDA UDI e8de5552-2592-484d-8641-ed7d26c93659 36 fields · synced May 30, 2026