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

Accessories, Retractor, Dental

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

EIF is the FDA product code for Accessories, Retractor, Dental, a class I device type, regulated under 21 CFR 872.4565. As of , FDA records hold 4 510(k) clearances under this code, the most recent dated , and no recalls.

Classification record

Product code
EIF
Device name
Accessories, Retractor, 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
4
Ingested recalls
0

Clearances, product code EIF

By decision year
4 clearances under product code EIF with a decision year between 1983 and 1994, 1983 the highest year at 2.
Show the numbers
510(k) clearances under FDA product code EIF by decision year
YearClearances
19832
19871
19941

Applicants with the most clearances

Product code EIF
Applicants holding the most 510(k) clearances under product code EIF
ApplicantClearances
Cheri Lewis, D.D.S.1
Hematology Marketing Assoc.1
North Pacific Dental, Inc.1
Worldwide Dental, Inc.1

Companies listing this code with FDA

Companies whose registered establishments list this code

12 of 162 companies shown, in name order