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restor3d Disposable Instrument, Cervical Cage Trial
FDA UDIClass I (US FDA UDI)
by Restor3D
Identity
- Trade Name
- restor3d Disposable Instrument, Cervical Cage Trial FDA UDI
- Generic Name
- Spinal implant trial FDA UDI
- Device Name
- Disposable Trial, Cervical Cage, Large Footprint, 12mm Thickness, 0 degrees FDA UDI
- Model / Reference
- 6110-17151200 FDA UDI
- Description
- Disposable Trial, Cervical Cage, Large Footprint, 12mm Thickness, 0 degrees FDA UDI
Identifiers
- Primary DI / UDI-DI
- 00840097501314 FDA UDI
- FDA Product Code
- LXH FDA UDI
- GMDN Term
- Spinal implant trial 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
Yes
FDA UDI
Single Use
Yes
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
Yes
FDA UDI
Lot / Batch Number
Yes
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
Yes
FDA UDI
Manufacturing Date
No
FDA UDI
Category: Spinal implant trial
restor3d Disposable Instrument, Cervical Cage Trial by Restor3D — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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Also classified as Spinal implant trial.
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- IdentiTi — ALPHATEC SPINE, INC. · Class II
- MLX — Nuvasive, Inc. · Class I
- IdentiTi — ALPHATEC SPINE, INC. · Class II
- ROI-A — Ldr Spine USA · Class II
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 I | Pending data |
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Manufacturer
- Manufacturer
- Restor3D
Sources (1)
- FDA UDI 79fe12fb-d7ec-431b-aa84-431bc046fb5c 33 fields · synced Jun 8, 2026