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

Syringe, Irrigating (Dental)

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

EIB is the FDA product code for Syringe, Irrigating (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
EIB
Device name
Syringe, Irrigating (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 EIB

By decision year
4 clearances under product code EIB with a decision year between 1976 and 1991, 1976 the highest year at 1.
Show the numbers
510(k) clearances under FDA product code EIB by decision year
YearClearances
19761
19831
19881
19911

Applicants with the most clearances

Product code EIB
Applicants holding the most 510(k) clearances under product code EIB
ApplicantClearances
Allergan1
Cp Medical1
Western Advanced Technology, Inc.1
Xomed, Inc.1

Companies listing this code with FDA

Companies whose registered establishments list this code

12 of 66 companies shown, in name order