Identity
- Trade Name
- ENDOSKELETON® TC nanoLOCK® Surface Technology FDA UDI
- Generic Name
- Metallic spinal interbody fusion cage FDA UDI
- Device Name
- Interbody Fusion Device Parallel Small 10mm FDA UDI
- Model / Reference
- 5140-1210-N FDA UDI
- Description
- Interbody Fusion Device Parallel Small 10mm FDA UDI
Identifiers
- Catalog Number
- 5140-1210-N FDA UDI
- Primary DI / UDI-DI
- 00191375012788 FDA UDI
- FDA Product Code
- ODP 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
- Depth — 12 Millimeter FDA UDIWidth — 14 Millimeter FDA UDIHeight — 10 Millimeter FDA UDI
Category: Metallic spinal interbody fusion cage
ENDOSKELETON® TC nanoLOCK® Surface Technology by Titan Spine, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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Also classified as Metallic spinal interbody fusion cage.
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- CoRoent — Nuvasive, Inc. · Class II
- Kyocera Medical Technologies, Inc. — Kyocera Medical Technologies, Inc. · Class II
- MectaLIF 3D — Medacta International · Class II
- PILLAR TL — Orthofix US LLC · Class II
- Solar™ Interbody Fusion System — Degen Medical · Class II
- Peridot-TD Anterior Cervical Intervertebral body fusion system — GBS Commonwealth Co., Ltd. · Class II
Cleared under the same submission
K100889 also covers:
- ENDOSKELETON® TC — MEDTRONIC SOFAMOR DANEK, INC.
- ENDOSKELETON® TC — MEDTRONIC SOFAMOR DANEK, INC.
- ENDOSKELETON® TC — MEDTRONIC SOFAMOR DANEK, INC.
- ENDOSKELETON® TC — MEDTRONIC SOFAMOR DANEK, INC.
- ENDOSKELETON® TC — MEDTRONIC SOFAMOR DANEK, INC.
- ENDOSKELETON® TC — MEDTRONIC SOFAMOR DANEK, INC.
- ENDOSKELETON® TC — MEDTRONIC SOFAMOR DANEK, INC.
- ENDOSKELETON® TC — MEDTRONIC SOFAMOR DANEK, INC.
- ENDOSKELETON® TC — Titan Spine, Inc.
- ENDOSKELETON® TC — Titan Spine, Inc.
- ENDOSKELETON® TC nanoLOCK® Surface Technology — Titan Spine, Inc.
- ENDOSKELETON® TC nanoLOCK® Surface Technology — Titan Spine, Inc.
K141953 also covers:
- ENDOSKELETON® TA nanoLOCK® Surface Technology — MEDTRONIC SOFAMOR DANEK, INC.
- ENDOSKELETON® TAS nanoLOCK® Surface Technology — MEDTRONIC SOFAMOR DANEK, INC.
- ENDOSKELETON® TC nanoLOCK® Surface Technology — MEDTRONIC SOFAMOR DANEK, INC.
- ENDOSKELETON® TL nanoLOCK® Surface Technology — MEDTRONIC SOFAMOR DANEK, INC.
- ENDOSKELETON® TO nanoLOCK® Surface Technology — MEDTRONIC SOFAMOR DANEK, INC.
- ENDOSKELETON® TC nanoLOCK® Surface Technology — Titan Spine, Inc.
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
- Titan Spine, Inc.
Sources (1)
- FDA UDI d240c648-0c8a-4fd2-b97e-c2fefb7c5427 37 fields · synced Jun 8, 2026