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

Syringe, Periodontic, Endodontic, Irrigating

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

EIC is the FDA product code for Syringe, Periodontic, Endodontic, Irrigating, a class I device type, regulated under 21 CFR 872.4565. As of , FDA records hold 16 510(k) clearances under this code, the most recent dated , and one recall.

Classification record

Product code
EIC
Device name
Syringe, Periodontic, Endodontic, Irrigating
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
16
Ingested recalls
1

Clearances, product code EIC

By decision year
16 clearances under product code EIC with a decision year between 1977 and 1997, 1977 the highest year at 4.
Show the numbers
510(k) clearances under FDA product code EIC by decision year
YearClearances
19774
19791
19804
19812
19841
19851
19862
19971

Applicants with the most clearances

Product code EIC
Applicants holding the most 510(k) clearances under product code EIC
ApplicantClearances
National Patent Development Corp.4
Aus-Tex Dental Mfg. & Design3
Dental Development Services, Inc.2
Centrix, Inc.1
Dentsply Intl.1
Smith & Nephew, Inc.1
Smith & Nephew, Mpl Division1
Solar Dental Co., Inc.1
Solo Pak Laboratories1
Suncoast Dental, Inc.1

Companies listing this code with FDA

Companies whose registered establishments list this code

12 of 138 companies shown, in name order