EZ BRUSH & FLOSS— 510(k) K873317

Name: FDA 510(k) clearance K873317
Creator: U.S. Food and Drug Administration
Published: 1988-01-19

Substantially Equivalent

Ez Products, Ltd.

FDA 510(k) clearance K873317 for EZ BRUSH & FLOSS, Substantially Equivalent on 1988-01-19. Applicant: Ez Products, Ltd.. Device class: 1.

Clearance details

Applicant: Ez Products, Ltd.
Product code: Code EFW
Device class: Class 1
Regulation: 21 CFR 872.6855
Advisory panel: Dental
Date received: 1987-08-19
Decision date: 1988-01-19
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Canada, CA

Download summary PDF View on FDA.gov ↗

Recent devices under product code EFW

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K130186 — DENTEK EASY BRUSH WITH FLUORIDE2013-07-15
K121165 — BEAM BRUSH/BEAM APP2012-06-21
K102871 — SILVER CARE ANITBACTERIAL TOOTHBRUSH2011-10-03
K073224 — ORAL-B SUB-BRAND MANUAL TOOTHBRUSH2008-02-06
K021383 — ZEODYNE TOOTHBRUSH WITH AGION ANTIMICROBIAL2002-07-17

Adverse events under product code EFW

product code EFW

Injury: 143
Malfunction: 698
Total: 841

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.