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
KZPClass II

Solution, Cement Dissolving

21 CFR 872.3750 / Dental
FDA source (opens on fda.gov)

KZP is the FDA product code for Solution, Cement Dissolving, a class II device type, regulated under 21 CFR 872.3750. As of , FDA records hold 2 510(k) clearances under this code, the most recent dated , and one recall.

Classification record

Product code
KZP
Device name
Solution, Cement Dissolving
Regulation
21 CFR 872.3750
Device class
Class II
Review panel
Dental
Submission type
510(k)
Implant
No
Life sustaining or supporting
No
GMP exempt
No
Third party review eligible
Yes
Ingested clearances
2
Ingested recalls
1

Clearances, product code KZP

By decision year
2 clearances under product code KZP with a decision year between 1978 and 1993, 1978 the highest year at 1.
Show the numbers
510(k) clearances under FDA product code KZP by decision year
YearClearances
19781
19931

Applicants with the most clearances

Product code KZP
Applicants holding the most 510(k) clearances under product code KZP
ApplicantClearances
Confi-Dental Products Co.1
Den-Mat Corp.1

Companies listing this code with FDA

Companies whose registered establishments list this code