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

Gauge, Depth, Instrument, Dental

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

EIL is the FDA product code for Gauge, Depth, Instrument, Dental, a class I device type, regulated under 21 CFR 872.4565. As of , FDA records hold 8 510(k) clearances under this code, the most recent dated , and no recalls.

Classification record

Product code
EIL
Device name
Gauge, Depth, Instrument, Dental
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
8
Ingested recalls
0

Clearances, product code EIL

By decision year
8 clearances under product code EIL with a decision year between 1982 and 1991, 1989 the highest year at 3.
Show the numbers
510(k) clearances under FDA product code EIL by decision year
YearClearances
19821
19872
19881
19893
19911

Applicants with the most clearances

Product code EIL
Applicants holding the most 510(k) clearances under product code EIL
ApplicantClearances
Abiomed, Inc.2
Bowen & Company, Inc.1
Dentsply Intl.1
Dr. Bernard Loewenthal1
Florida Probe Corp.1
National Patent Development Corp.1
Vine Valley Research1

Companies listing this code with FDA

Companies whose registered establishments list this code

12 of 140 companies shown, in name order