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

Laser Activator For Polymerization

21 CFR 872.6070 / Dental
FDA source (opens on fda.gov)

QNF is the FDA product code for Laser Activator For Polymerization, a class II device type, regulated under 21 CFR 872.6070. FDA's definition for this code reads: "Intended to polymerize dental restorative resins". As of , FDA records hold 2 510(k) clearances under this code, the most recent dated , and no recalls.

Classification record

Product code
QNF
Device name
Laser Activator For Polymerization
FDA definition
Intended to polymerize dental restorative resins
Regulation
21 CFR 872.6070
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
No
Ingested clearances
2
Ingested recalls
0

Clearances, product code QNF

By decision year
2 clearances under product code QNF with a decision year between 2020 and 2023, 2020 the highest year at 1.
Show the numbers
510(k) clearances under FDA product code QNF by decision year
YearClearances
20201
20231

Applicants with the most clearances

Product code QNF
Applicants holding the most 510(k) clearances under product code QNF
ApplicantClearances
Cao Group, Inc.1
Lumendo AG1

Companies listing this code with FDA

Companies whose registered establishments list this code