510(k) Report

FDA applicant

Attachments Intl., Inc.

San Mateo, CA2 decisions1991–19910 recalls

FDA records 2 decisions for Attachments Intl., Inc. (San Mateo, CA) in 1991: 2 510(k) clearances. All are in product code DZE (Implant, Endosseous, Root-Form). No recall is linked to its devices.

Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) refreshed weekly, last Nov 3, 2026

FIG. A — Illustration, dental panel, where it files most

How often FDA has decided Attachments Intl., Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Attachments Intl., Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Attachments Intl., Inc. by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

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Which product codes does it file in?

  • DZEImplant, Endosseous, Root-Form2decisions

Who builds on its devices?

Later devices cite its devices 1 time; 0 of those are its own. The firms that cite it most:

Which of its devices are cited most?

Its devices that later submissions most often claim equivalence to.

  • K900099The O-Ring System - OrsAttachments Intl., Inc. · 19911cites it

What has FDA decided for it lately?

  • K904236Endosseous ImplantsAttachments Intl., Inc. · 1991
  • K900099The O-Ring System - OrsAttachments Intl., Inc. · 1991

All 2 as Attachments Intl., Inc. →