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
EIRClass I

Scissors, Collar And Crown

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

EIR is the FDA product code for Scissors, Collar And Crown, 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
EIR
Device name
Scissors, Collar And Crown
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 EIR

By decision year
1 clearance under product code EIR with a decision year between 1985 and 1985, 1985 the highest year at 1.
Show the numbers
510(k) clearances under FDA product code EIR by decision year
YearClearances
19851

Applicants with the most clearances

Product code EIR
Applicants holding the most 510(k) clearances under product code EIR
ApplicantClearances
Artiberia1

Companies listing this code with FDA

Companies whose registered establishments list this code

12 of 83 companies shown, in name order