510(k) Report

FDA applicant

Iq Implants, Ltd.

Omer, IL1 decision2013–20130 recalls

FDA records 1 decision for Iq Implants, Ltd. (Omer, IL) in 2013: 1 510(k) clearance. 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 Iq Implants, Ltd.’s devices, and how often a recall has named them.

FDA decisions per year

1in 2013

2013: 1
2013high 1 (2013) · low 0 (2014)2026

2026 so far, outlined.

Recalls per year

No recall linked to its devices since 2013.

FIG. 1 — Iq Implants, Ltd. by year, 2013–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

Planning a device like Iq Implants, Ltd.’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-Form1decision

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.

  • K130829IQ Implants; IQ Implants; IQ Implants AbutmentsIq Implants, Ltd. · 20131cites it

What has FDA decided for it lately?

  • K130829IQ Implants; IQ Implants; IQ Implants AbutmentsIq Implants, Ltd. · 2013

The one decision as Iq Implants, Ltd. →