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Secure Implant System(2.5/3.0mm)

FDA UDI

Class II (US FDA UDI)

by DIO Corporation

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
MICP 3511 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
MICP 3511 FDA UDI
Primary DI / UDI-DI
08806195929872 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

Secure Implant System(2.5/3.0mm) by DIO Corporation — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
DIO Corporation

Sources (1)

  • FDA UDI 09f4a346-762b-4fb5-882c-11f9c41dd90e 38 fields · synced May 31, 2026