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

System, Dental, Hydrokinetic, Caries Removal & Cavity Preparation

21 CFR 872.4120 / Dental
FDA source (opens on fda.gov)

MXF is the FDA product code for System, Dental, Hydrokinetic, Caries Removal & Cavity Preparation, a class II device type, regulated under 21 CFR 872.4120. As of , FDA records hold 5 510(k) clearances under this code, the most recent dated , and no recalls.

Classification record

Product code
MXF
Device name
System, Dental, Hydrokinetic, Caries Removal & Cavity Preparation
Regulation
21 CFR 872.4120
Device class
Class II
Review panel
Dental
Submission type
510(k)
Implant
No
Life sustaining or supporting
No
GMP exempt
No
Third party review eligible
Yes
Ingested clearances
5
Ingested recalls
0

Clearances, product code MXF

By decision year
5 clearances under product code MXF with a decision year between 1999 and 2003, 1999 the highest year at 2.
Show the numbers
510(k) clearances under FDA product code MXF by decision year
YearClearances
19992
20022
20031

Applicants with the most clearances

Product code MXF
Applicants holding the most 510(k) clearances under product code MXF
ApplicantClearances
Biolase MG LLC4
Endo Technic Corp.1

Companies listing this code with FDA

Companies whose registered establishments list this code