510(k) Report

FDA applicant

Saber Technology, Inc.

Seattle, WA2 decisions1988–19940 recalls

FDA records 2 decisions for Saber Technology, Inc. (Seattle, WA) from 1988 to 1994: 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 Saber Technology, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Saber Technology, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like Saber Technology, Inc.’s? A 510(k) Report ranks candidate predicates for your device by lineage, citations and recall history, with the review-time outlook.

See the 510(k) Report

Which product codes does it file in?

  • DZEImplant, Endosseous, Root-Form2decisions

Who builds on its devices?

Later devices cite its devices 3 times; 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.

  • K924112Hydroxylapatite Coated Saber Tech Series I & Series IISaber Technology, Inc. · 19943cite it

What has FDA decided for it lately?

  • K924112Hydroxylapatite Coated Saber Tech Series I & Series IISaber Technology, Inc. · 1994
  • K882226Series I and II ImplantsSaber Technology, Inc. · 1988

All 2 as Saber Technology, Inc. →