Identity
- Trade Name
- SECURE IMPLANT SYSTEM(2.5/3.0MM) FDA UDI
- Generic Name
- Screw endosteal dental implant, two-piece FDA UDI
- Device Name
- Secure Implant System(2.5/3.0MM) is a root-form threaded dental implant made of titanium alloy. The implant is produced by machining process, followed by grit blasting and cleaning. It is available in diameters 2.5 and 3.0mm, and lengths from 8mm to 16mm. FDA UDI
- Model / Reference
- MAB 3014 FDA UDI
- Description
- Secure Implant System(2.5/3.0MM) is a root-form threaded dental implant made of titanium alloy. The implant is produced by machining process, followed by grit blasting and cleaning. It is available in diameters 2.5 and 3.0mm, and lengths from 8mm to 16mm. FDA UDI
Identifiers
- Catalog Number
- MAB 3014 FDA UDI
- Primary DI / UDI-DI
- 08806195916599 FDA UDI
- FDA Product Code
- NHA FDA UDI
- GMDN Term
- Screw endosteal dental implant, two-piece FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 872.3630 FDA UDI
- Commercial Distribution
- Not 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
Yes
FDA UDI
Expiration Date
Yes
FDA UDI
Manufacturing Date
Yes
FDA UDI
The Secure Implant System(2.5/3.0MM) is a high-quality, two-piece dental implant made of titanium alloy. This implant is designed to provide support and retention for dental prosthesis (e.g., bridge, single-tooth, overdenture) in the mandible or maxilla. With a durable design and precise machining process, it's ideal for patients seeking a long-lasting solution.
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
- DIO Corporation
Sources (1)
- FDA UDI 1286ea41-942a-4d01-9c30-5d852312109c 38 fields · synced Jul 24, 2026