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

Toothbrush, Ionic, Battery-Powered

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

MMD is the FDA product code for Toothbrush, Ionic, Battery-Powered, a class I device type, regulated under 21 CFR 872.6865. As of , FDA records hold 2 510(k) clearances under this code, the most recent dated , and 5 recalls.

Classification record

Product code
MMD
Device name
Toothbrush, Ionic, Battery-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
2
Ingested recalls
5

Clearances, product code MMD

By decision year
2 clearances under product code MMD with a decision year between 1994 and 1997, 1994 the highest year at 1.
Show the numbers
510(k) clearances under FDA product code MMD by decision year
YearClearances
19941
19971

Applicants with the most clearances

Product code MMD
Applicants holding the most 510(k) clearances under product code MMD
ApplicantClearances
Hukuba Dental Corp.1
SAS Group, Inc.1

Companies listing this code with FDA

Companies whose registered establishments list this code

12 of 37 companies shown, in name order