Consulting Wallah › Device Explorer › Dental › Magnetic dental precision attachment
Device Explorer · FDA GUDID · GMDN 38578

Magnetic dental precision attachment

A device with magnetic properties designed for fixation of a removable dental prosthesis.

US‑registered devices203in commercial distribution
Companies2labelers on GUDID
Single‑use90%of device records
Sterile0%labelled sterile
Prescription59%Rx‑only share
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Share of device records

Steco-System-Technik Gmbh & Co Kg12662%
Technovent Limited7738%

Top labelers

CompanyDevicesShare
Steco-System-Technik Gmbh & Co Kg12662%
Technovent Limited7738%

Company = labeler of record on GUDID. 2 companies in total; top 12 shown. Click headers to sort.

Brand names on the register (sample)

‘MagnaCap’ Magnetic Retention SystemMagnabutmentsStecoTitanmagnetics®

Sample of brand names as labelled; no endorsement. Ask us for the full list with company, model and UDI.

FDA product codes

CodeNameDevices
EGGAttachment, Precision, All167
KCZProsthesis, Breast, External, Used With Adhesive77
DZEImplant, Endosseous, Root-Form16
EGGATTACHMENT, PRECISION, ALL12

GMDN & GCC registration

  • GMDN code 38578 · non‑implantable
  • Single‑use 90% · sterile 0% · Rx‑only 59% · OTC 0%
  • UAE: MOHAP / DoH medical device registration and an authorised representative are required; Saudi: SFDA MDMA. We check status on request.

Size attributes recorded

No structured size data on the register.

Use these as the dimensions to specify in a tender line.

How many magnetic dental precision attachment products are registered in the US?

203 device records in commercial distribution are listed on the FDA Global Unique Device Identification Database (GUDID) under the GMDN category "Magnetic dental precision attachment", from 2 companies. The largest labeler is Steco-System-Technik Gmbh & Co Kg with 62% of records.

Which FDA product codes apply?

EGG (Attachment, Precision, All), KCZ (Prosthesis, Breast, External, Used With Adhesive), DZE (Implant, Endosseous, Root-Form), EGG (ATTACHMENT, PRECISION, ALL)

Is this the same as UAE/GCC registration?

No. GUDID is the US register. For the UAE (MOHAP/DoH) and Saudi (SFDA/MDMA) a separate registration and a local authorised representative are required; Consulting Wallah can check the status and connect you with registered suppliers.

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Source: FDA AccessGUDID (AccessGUDID full release 2 Nov 2026); counts are device records in commercial distribution grouped by GMDN preferred term; companies are labelers of record. Information only — US listing is not a registration in the UAE or GCC; verify with the regulator. © Consulting Wallah — CC BY‑NC‑ND.

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