Identity
- Trade Name
- ENCLAVE™ ANTERIOR SPINAL SYSTEM FDA UDI
- Generic Name
- Vertebral body prosthesis FDA UDI
- Model / Reference
- 14-530580 FDA UDI
Identifiers
- Catalog Number
- 14-530580 FDA UDI
- Primary DI / UDI-DI
- 00880304911222 FDA UDI
- FDA Product Code
- MAX FDA UDI
- GMDN Term
- Vertebral body prosthesis 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
No
FDA UDI
Manufacturing Date
No
FDA UDI
Category: Vertebral body prosthesis
Enclave™ Anterior Spinal System by Biomet Spine Llc — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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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
- Biomet Spine Llc
Sources (1)
- FDA UDI 63eaa309-d426-4b35-af50-f0a4b2cd1efb 35 fields · synced May 30, 2026