510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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JEQClass I

Toothbrush, Powered

21 CFR 872.6865 / Dental
FDA source (opens on fda.gov)

JEQ is the FDA product code for Toothbrush, Powered, a class I device type, regulated under 21 CFR 872.6865. As of , FDA records hold 54 510(k) clearances under this code, the most recent dated , and 36 recalls.

Classification record

Product code
JEQ
Device name
Toothbrush, Powered
Regulation
21 CFR 872.6865
Device class
Class I
Review panel
Dental
Submission type
510(k) exempt
Implant
No
Life sustaining or supporting
No
GMP exempt
No
Third party review eligible
No
Ingested clearances
54
Ingested recalls
36

Clearances, product code JEQ

By decision year
54 clearances under product code JEQ with a decision year between 1977 and 2020, 1994 the highest year at 10.
Show the numbers
510(k) clearances under FDA product code JEQ by decision year
YearClearances
19772
19781
19812
19822
19853
19863
19872
19881
19891
19906
19913
19924
19934
199410
19952
19971
20011
20021
20041
20062
20141
20201

Applicants with the most clearances

Product code JEQ
Applicants holding the most 510(k) clearances under product code JEQ
ApplicantClearances
American Dentronics, Inc.3
Bausch & Lomb Incorporated2
Braun GmbH2
John O. Butler Co.2
Omron Healthcare Co., Ltd.2
Procter & Gamble Co.2
Anco Merchandise Co., Ltd.1
Brilliant Industries, Inc.1
Crossroads Trading Co.1
Dental Research Corp.1

Companies listing this code with FDA

Companies whose registered establishments list this code

12 of 346 companies shown, in name order