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
EGIClass I

Parallelometer

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

EGI is the FDA product code for Parallelometer, a class I device type, regulated under 21 CFR 872.4565. As of , FDA records hold one 510(k) clearance under this code, the most recent dated , and no recalls.

Classification record

Product code
EGI
Device name
Parallelometer
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
1
Ingested recalls
0

Clearances, product code EGI

By decision year
1 clearance under product code EGI with a decision year between 1980 and 1980, 1980 the highest year at 1.
Show the numbers
510(k) clearances under FDA product code EGI by decision year
YearClearances
19801

Applicants with the most clearances

Product code EGI
Applicants holding the most 510(k) clearances under product code EGI
ApplicantClearances
C.D. Charles, Inc.1

Companies listing this code with FDA

Companies whose registered establishments list this code