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Diamodent

FDA UDI

Class II (US FDA UDI)

by Diamodent

Identity

Trade Name
Diamodent FDA UDI
Generic Name
Dental implant suprastructure, permanent, preformed FDA UDI
Device Name
Compatible with: 3.5mm Narrow Platform (NP) NobelReplace implants Cement-On Post, Titanium 4mm Collar, 4.5mm Profile, Titefit FDA UDI
Model / Reference
N/A FDA UDI
Description
Compatible with: 3.5mm Narrow Platform (NP) NobelReplace implants Cement-On Post, Titanium 4mm Collar, 4.5mm Profile, Titefit FDA UDI

Identifiers

Catalog Number
AA515 FDA UDI
Primary DI / UDI-DI
D907AA5150 FDA UDI
FDA Product Code
DZE FDA UDI
GMDN Term
Dental implant suprastructure, permanent, preformed FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
872.3640 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

No

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
Sterilization Method
Dry Heat Sterilization FDA UDI

Category: Dental implant suprastructure, permanent, preformed

Diamodent by Diamodent — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Dental implant suprastructure, permanent, preformed.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Diamodent

Sources (1)

  • FDA UDI 873211cb-b10a-4bfc-bc04-b3f0ee6f2434 34 fields · synced Jun 1, 2026