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

Clamp, Rubber Dam

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

EEF is the FDA product code for Clamp, Rubber Dam, a class I device type, regulated under 21 CFR 872.6300. As of , FDA records hold 3 510(k) clearances under this code, the most recent dated , and one recall.

Classification record

Product code
EEF
Device name
Clamp, Rubber Dam
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
3
Ingested recalls
1

Clearances, product code EEF

By decision year
3 clearances under product code EEF with a decision year between 1978 and 2007, 1978 the highest year at 1.
Show the numbers
510(k) clearances under FDA product code EEF by decision year
YearClearances
19781
19921
20071

Applicants with the most clearances

Product code EEF
Applicants holding the most 510(k) clearances under product code EEF
ApplicantClearances
Bay Technical Products, Inc.1
Hygienic Dental Mfg., Co., the1
Sybron Dental Specialties, Inc.1

Companies listing this code with FDA

Companies whose registered establishments list this code

12 of 96 companies shown, in name order