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
EHZClass I

Evacuator, Oral Cavity

21 CFR 872.6640 / Dental
FDA source (opens on fda.gov)

EHZ is the FDA product code for Evacuator, Oral Cavity, a class I device type, regulated under 21 CFR 872.6640. As of , FDA records hold 17 510(k) clearances under this code, the most recent dated , and one recall.

Classification record

Product code
EHZ
Device name
Evacuator, Oral Cavity
Regulation
21 CFR 872.6640
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
17
Ingested recalls
1

Clearances, product code EHZ

By decision year
17 clearances under product code EHZ with a decision year between 1977 and 1997, 1978 the highest year at 3.
Show the numbers
510(k) clearances under FDA product code EHZ by decision year
YearClearances
19771
19783
19791
19801
19861
19873
19881
19892
19901
19911
19941
19971

Applicants with the most clearances

Product code EHZ
Applicants holding the most 510(k) clearances under product code EHZ
ApplicantClearances
Dentsply Intl.2
Nieusma R & D, Inc.2
A & F Products1
Columbus Dental Mfg. Co.1
Commercial Products & Engineering Co.1
Cpac, Inc.1
Cygnus Instruments, Inc.1
Dental Innovators, Inc.1
Implant Innovations International, Inc.1
Imtec Corp.1

Companies listing this code with FDA

Companies whose registered establishments list this code

12 of 136 companies shown, in name order