Identity
- Trade Name
- ENDOSKELETON TL RETRACTOR FDA UDI
- Generic Name
- Surgical retraction system, reusable FDA UDI
- Device Name
- Reusable Light Connector FDA UDI
- Model / Reference
- R14154-15 FDA UDI
- Description
- Reusable Light Connector FDA UDI
Identifiers
- Catalog Number
- R14154-15 FDA UDI
- Primary DI / UDI-DI
- M682R141542150 FDA UDI
- FDA Product Code
- FST FDA UDI
- GMDN Term
- Surgical retraction system, reusable FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 878.4580 FDA UDI
- Commercial Distribution
- Not 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
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
No
FDA UDI
Manufacturing Date
Yes
FDA UDI
Moist Heat or Steam Sterilization FDA UDI
Endoskeleton Tl Retractor by Titan Spine, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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 faba1bb8-4f8d-4636-9b16-84958ae04171 36 fields · synced Jun 1, 2026