← FDA DEVICE PRODUCT CODES

FDA PRODUCT CODE · CLASS II

DZJ — Driver, Wire, And Bone Drill, Manual

DEVICE CLASS
Class II
REGULATION
21 CFR 872.4120
MEDICAL SPECIALTY
Dental
REVIEW PANEL
DE
— Implant— Life-sustaining— GMP-exempt✓ Third-party review eligible
3
510(K)/PMA CLEARANCES
510k: 3
0
RECALL ENTRIES

Recent clearances

K2618263D Systems, Inc. · 510k2026-06-03
K243637Materialise NV · 510k2025-02-21
K242263Techfit Digital Surgery, Inc. · 510k2024-12-11

Related on SPEQ

Medical devices industry →Medical device quality (ISO 13485) →FDA device clearances →FDA enforcement & recalls →

Source: FDA device classification, 510(k)/PMA, and recall datasets (openFDA). Recall entries count distinct FDA recall numbers, so one recall event affecting several products appears as several entries. SPEQ is not affiliated with the FDA; this is a reference view of public FDA data.

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