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Secure-C

FDA UDI

Class III (US FDA UDI)

by Globus Medical, Inc.

Identity

Trade Name
SECURE-C FDA UDI
Generic Name
Cervical total intervertebral disc prosthesis, modular FDA UDI
Device Name
SECURE-C Core, 11x12, 9mm FDA UDI
Model / Reference
414.109S FDA UDI
Description
SECURE-C Core, 11x12, 9mm FDA UDI

Identifiers

Primary DI / UDI-DI
00889095154818 FDA UDI
PMA Number
P100003 FDA UDI
FDA Product Code
MJO FDA UDI
GMDN Term
Cervical total intervertebral disc prosthesis, modular FDA UDI

Classification

Device Class
Class III 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

No

FDA UDI

Dimensions & Sizes

Size
Depth — 11 Millimeter FDA UDI
Width — 12 Millimeter FDA UDI
Height — 9 Millimeter FDA UDI

Category: Cervical total intervertebral disc prosthesis, modular

Secure-C by Globus Medical, Inc. — Class III — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Cervical total intervertebral disc prosthesis, modular.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI f08932d0-f3bf-4647-a75b-e16f08e71a00 36 fields · synced May 30, 2026