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

Forceps, Rubber Dam Clamp

21 CFR 872.6300 / Dental
FDA source (opens on fda.gov)

EJG is the FDA product code for Forceps, Rubber Dam Clamp, a class I device type, regulated under 21 CFR 872.6300. As of , FDA records hold one 510(k) clearance under this code, the most recent dated , and 4 recalls.

Classification record

Product code
EJG
Device name
Forceps, Rubber Dam Clamp
Regulation
21 CFR 872.6300
Device class
Class I
Review panel
Dental
Submission type
510(k) exempt
Implant
No
Life sustaining or supporting
No
GMP exempt
Yes
Third party review eligible
No
Ingested clearances
1
Ingested recalls
4

Clearances, product code EJG

By decision year
1 clearance under product code EJG with a decision year between 1978 and 1978, 1978 the highest year at 1.
Show the numbers
510(k) clearances under FDA product code EJG by decision year
YearClearances
19781

Applicants with the most clearances

Product code EJG
Applicants holding the most 510(k) clearances under product code EJG
ApplicantClearances
Hygienic Dental Mfg., Co., the1

Companies listing this code with FDA

Companies whose registered establishments list this code

12 of 102 companies shown, in name order