QQFNot classified

Skin Microneedling Manual/Automated Device (Export Only)

Unknown

QQF is the FDA product code for Skin Microneedling Manual/Automated Device (Export Only). FDA's definition for this code reads: "For one-time (1X) use by qualified clinical professionals to cause bio-active effect(s) in skin for aesthetic improvement". As of 2026-09-10, FDA records hold no 510(k) clearances under this code and no recalls.

Classification record

Product code: QQF
Device name: Skin Microneedling Manual/Automated Device (Export Only)
FDA definition: For one-time (1X) use by qualified clinical professionals to cause bio-active effect(s) in skin for aesthetic improvement.
Device class: Not classified
Review panel: Unknown
Submission type: Contact ODE
Implant: No
Life sustaining or supporting: No
GMP exempt: No
Third party review eligible: No
Ingested clearances: 0
Ingested recalls: 0

Companies listing this code with FDA

Companies whose registered establishments list this code

Clinical Resolution Laboratory, Inc.

Recent clearances

Product code QQF

FDA records hold no clearances under product code QQF.

Recent recalls

Product code QQF

FDA records show no recalls under product code QQF.

MDM coverage of this record lists here, newest first.

About this record

Sourced from the FDA device classification database, ingested from openFDA. The definition, regulation number, device class and review panel are FDA’s own fields, reproduced without editing.

MDM adds the counts: clearances by decision year, the applicants holding the most clearances under this code, recalls that name it, and the registered establishments that list it. Every count is computed from ingested records only.

Data as of 2026-10-05, the FDA export date for this dataset. Page last changed 2026-09-05. View this product code on fda.gov (opens on fda.gov)