DeviceClearance

Product code DZL— Dental

THE AUTOTAC SYSTEM

Classification name
Screw, Fixation, Intraosseous
Device class
Class 2
Regulation
21 CFR 872.4880
Advisory panel
Dental
Total cleared
81
First cleared
Most recent

Market context for product code DZL

FDA has cleared 81 devices under product code DZL between 1976 and 2026, filed by 44 applicant companies. No FDA device recalls reference this product code. Class II devices are moderate-risk and subject to general and special controls; most reach market through 510(k) clearance by demonstrating substantial equivalence to a predicate device.

Clearances per year

last 15 years

Top applicants under product code DZL

Adverse events under product code DZL

product code DZL
Injury
168
Total
168

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

Recent clearances under product code DZL

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