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Magnabutments

FDA UDI

Class II (US FDA UDI)

by Technovent Limited

Identity

Trade Name
Magnabutments FDA UDI
Generic Name
Magnetic dental precision attachment FDA UDI
Device Name
Technovent Magnabutments are a form of magnetisable keeper which screw directly into a third party implant as part of a magnetic attachment system for implant retained craniofacial prostheses. FDA UDI
Model / Reference
P-MA2-6.5-S Maxi Magnabutment (Medicon, 6.5mm) – S-Range FDA UDI
Description
Technovent Magnabutments are a form of magnetisable keeper which screw directly into a third party implant as part of a magnetic attachment system for implant retained craniofacial prostheses. FDA UDI

Identifiers

Catalog Number
P-MA2-6.5-S FDA UDI
Primary DI / UDI-DI
05060483010656 FDA UDI
FDA Product Code
DZE FDA UDI
GMDN Term
Magnetic dental precision attachment 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

Yes

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

No

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

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI
MRI Safety
MR Unsafe FDA UDI

Category: Magnetic dental precision attachment

Magnabutments by Technovent Limited — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Magnetic dental precision attachment.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Technovent Limited

Sources (1)

  • FDA UDI 665bee50-27b7-4f8d-adcc-25039c36380a 35 fields · synced Jun 8, 2026