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

Eraser, Dental Stain

21 CFR 872.6855 / Dental
FDA source (opens on fda.gov)

MAU is the FDA product code for Eraser, Dental Stain, a class I device type, regulated under 21 CFR 872.6855. As of , FDA records hold 2 510(k) clearances under this code, the most recent dated , and one recall.

Classification record

Product code
MAU
Device name
Eraser, Dental Stain
Regulation
21 CFR 872.6855
Device class
Class I
Review panel
Dental
Submission type
510(k) exempt
Implant
No
Life sustaining or supporting
No
GMP exempt
Yes
Third party review eligible
No
Ingested clearances
2
Ingested recalls
1

Clearances, product code MAU

By decision year
2 clearances under product code MAU with a decision year between 1989 and 2000, 1989 the highest year at 1.
Show the numbers
510(k) clearances under FDA product code MAU by decision year
YearClearances
19891
20001

Applicants with the most clearances

Product code MAU
Applicants holding the most 510(k) clearances under product code MAU
ApplicantClearances
The Precident Group1
The Smylon Co.1

Companies listing this code with FDA

Companies whose registered establishments list this code

12 of 64 companies shown, in name order