IMZ - DENTAL IMPLANT CASTABLE CSR ATTACHMENT— 510(k) K951617

Name: FDA 510(k) clearance K951617
Creator: U.S. Food and Drug Administration
Published: 1995-07-26

Substantially Equivalent

Imz, GmbH

FDA 510(k) clearance K951617 for IMZ - DENTAL IMPLANT CASTABLE CSR ATTACHMENT, Substantially Equivalent on 1995-07-26. Applicant: Imz, GmbH. Device class: 2.

Clearance details

Applicant: Imz, GmbH
Product code: Code DZE
Device class: Class 2
Regulation: 21 CFR 872.3640
Advisory panel: Dental
Date received: 1995-04-07
Decision date: 1995-07-26
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Potomac, MD, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code DZE

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K260463 — ZEROS Dental Implant System2026-08-19
K251188 — UNIQA® Dental Implants System2026-06-25
K250806 — Dental Implant System2026-06-18
K251232 — MegaGen Zygoma Dental Implant System2026-06-18
K260006 — INOSS System2026-06-17

More clearances from Imz, GmbH

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K963520 — IMZ TWIN PLUS SCREW1997-08-12
K963521 — IMZ TWIN PLUS - CYLINDER1997-08-06
K963495 — IMZ 2000 INTERLOCK 12/3 - CYLINDER DENTAL IMPLANT SYSTEM1997-03-03
K963522 — IMZ 2000 INTERLOCK 12/3 - SCREW1997-03-03
K951609 — IMZ - DENTAL IMPLANT SURGICAL TRAY1995-08-01

Adverse events under product code DZE

product code DZE

Death: 28
Injury: 3,367,041
Malfunction: 19,958
Other: 13
Total: 3,387,040

Source: openFDA MAUDE database, 2020-01-01 through 2026-04-23. Counts aggregate all devices under this product code, not just this specific clearance. Reports are submissions to FDA, not validated events. Search MAUDE directly →

Data sourced from openFDA. This site is unofficial and independent of the FDA.