DX TOOTHBRUSH— 510(k) K781018

Name: FDA 510(k) clearance K781018
Creator: U.S. Food and Drug Administration
Published: 1978-06-30

Substantially Equivalent

Lever Brothers Company, Inc.

FDA 510(k) clearance K781018 for DX TOOTHBRUSH, Substantially Equivalent on 1978-06-30. Applicant: Lever Brothers Company, Inc.. Device class: 1.

Clearance details

Applicant: Lever Brothers Company, Inc.
Product code: Code EFW
Device class: Class 1
Regulation: 21 CFR 872.6855
Advisory panel: Dental
Date received: 1978-06-16
Decision date: 1978-06-30
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

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

More clearances from Lever Brothers Company, Inc.

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K850610 — PEPSODENT DENTURE ADHESIVE CREAM1985-05-15
K851182 — PEPSODENT DENTURE CLEANSER-WESTONE FORMULA1985-04-29
K851183 — PEPSODENT DENTURE CLEANSER PDP FORMULA1985-04-29

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.