CAMLOG ROOTFORM IMPLANT SYSTEM— 510(k) K000100

Name: FDA 510(k) clearance K000100
Creator: U.S. Food and Drug Administration
Published: 2000-01-28

Substantially Equivalent

Altatec Biotechnologies

FDA 510(k) clearance K000100 for CAMLOG ROOTFORM IMPLANT SYSTEM, Substantially Equivalent on 2000-01-28. Applicant: Altatec Biotechnologies. Device class: 2.

Clearance details

Applicant: Altatec Biotechnologies
Product code: Code DZE
Device class: Class 2
Regulation: 21 CFR 872.3640
Advisory panel: Dental
Date received: 2000-01-13
Decision date: 2000-01-28
Decision: Substantially Equivalent
Clearance type: Special
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 Altatec Biotechnologies

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K032448 — ALTATEC CERAMIC ABUTMENT2003-08-22
K000065 — CAMLOG CYLINDER IMPLANT SYSTEM2000-01-28
K000099 — CAMLOG SCREW IMPLANT SYSTEM2000-01-28

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.