Identity
- Trade Name
- TALOS® IBF FDA UDI
- Generic Name
- Spinal implant trial FDA UDI
- Model / Reference
- 100-30909-25 FDA UDI
Identifiers
- Primary DI / UDI-DI
- B16710030909250 FDA UDI
- FDA Product Code
- MAX FDA UDI
- GMDN Term
- Spinal implant trial 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
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
Yes
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
No
FDA UDI
Moist Heat or Steam Sterilization FDA UDI
Category: Spinal implant trial
Talos® Ibf by Meditech Spine, Llc — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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Also classified as Spinal implant trial.
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Cleared under the same submission
K090707 also covers:
- TALOS® IBF — MEDITECH SPINE, LLC
- TALOS® IBF — MEDITECH SPINE, LLC
- TALOS® IBF — MEDITECH SPINE, LLC
- TALOS® IBF — MEDITECH SPINE, LLC
- TALOS® IBF — MEDITECH SPINE, LLC
- TALOS® IBF — MEDITECH SPINE, LLC
- TALOS® IBF — MEDITECH SPINE, LLC
- TALOS® IBF — MEDITECH SPINE, LLC
- TALOS® IBF — MEDITECH SPINE, LLC
- TALOS® IBF — MEDITECH SPINE, LLC
- TALOS® IBF — MEDITECH SPINE, LLC
- TALOS® IBF — MEDITECH SPINE, LLC
K150788 also covers:
- TALOS® IBF — MEDITECH SPINE, LLC
- TALOS® IBF — MEDITECH SPINE, LLC
- TALOS® IBF — MEDITECH SPINE, LLC
- TALOS® IBF — MEDITECH SPINE, LLC
- TALOS® IBF — MEDITECH SPINE, LLC
- TALOS® IBF — MEDITECH SPINE, LLC
- TALOS® IBF — MEDITECH SPINE, LLC
- TALOS® IBF — MEDITECH SPINE, LLC
- TALOS® IBF — MEDITECH SPINE, LLC
- TALOS® IBF — MEDITECH SPINE, LLC
- TALOS® IBF — MEDITECH SPINE, LLC
- TALOS® IBF — MEDITECH SPINE, LLC
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 |
Is this your device? Claim it to add documentation and request validation.
Manufacturer
- Manufacturer
- Meditech Spine, Llc
Sources (1)
- FDA UDI 374d0652-3c61-4041-a3bb-6b3da0190471 33 fields · synced Jun 1, 2026