510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
Medical Device
ManufacturingTHE TRADE PAPER OF THE FACTORY FLOOR
SUBSCRIBE / SIGN IN
EBPClass II

Reliner, Denture, Over The Counter

21 CFR 872.3560 / Dental
FDA source (opens on fda.gov)

EBP is the FDA product code for Reliner, Denture, Over The Counter, a class II device type, regulated under 21 CFR 872.3560. As of , FDA records hold 3 510(k) clearances under this code, the most recent dated , and no recalls.

Classification record

Product code
EBP
Device name
Reliner, Denture, Over The Counter
Regulation
21 CFR 872.3560
Device class
Class II
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
3
Ingested recalls
0

Clearances, product code EBP

By decision year
3 clearances under product code EBP with a decision year between 1979 and 2012, 1979 the highest year at 1.
Show the numbers
510(k) clearances under FDA product code EBP by decision year
YearClearances
19791
20101
20121

Applicants with the most clearances

Product code EBP
Applicants holding the most 510(k) clearances under product code EBP
ApplicantClearances
Den-Mat Corp.1
Majestic Drug Co., Inc.1
Perma Laboratories1

Companies listing this code with FDA

Companies whose registered establishments list this code