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

Probe, Periodontic

21 CFR 872.4565 / Dental
FDA source (opens on fda.gov)

EIX is the FDA product code for Probe, Periodontic, a class I device type, regulated under 21 CFR 872.4565. As of , FDA records hold 9 510(k) clearances under this code, the most recent dated , and no recalls.

Classification record

Product code
EIX
Device name
Probe, Periodontic
Regulation
21 CFR 872.4565
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
9
Ingested recalls
0

Clearances, product code EIX

By decision year
9 clearances under product code EIX with a decision year between 1982 and 1996, 1987 the highest year at 2.
Show the numbers
510(k) clearances under FDA product code EIX by decision year
YearClearances
19821
19872
19882
19891
19942
19961

Applicants with the most clearances

Product code EIX
Applicants holding the most 510(k) clearances under product code EIX
ApplicantClearances
Accudent, Inc.1
Alpkem Corp.1
Florida Probe Corp.1
Miltex, Inc.1
Pd International AB1
Periodontal Health Brush, Inc.1
Pro-Dentec1
Rms Div.1
Sweet Micro Systems, Inc.1

Companies listing this code with FDA

Companies whose registered establishments list this code

12 of 165 companies shown, in name order