NXFClass I

Gas, Laser Generating

21 CFR 878.4810 / General, Plastic Surgery

NXF is the FDA product code for Gas, Laser Generating, a class I device type, regulated under 21 CFR 878.4810. FDA's definition for this code reads: "Special laser gas mixtures used as a lasing medium". As of 2026-09-10, FDA records hold no 510(k) clearances under this code and no recalls.

Classification record

Product code: NXF
Device name: Gas, Laser Generating
FDA definition: Special laser gas mixtures used as a lasing medium
Regulation: 21 CFR 878.4810
Device class: Class I
Review panel: General, Plastic Surgery
Submission type: 510(k) exempt
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

12 of 35 companies shown, in name order

Recent clearances

Product code NXF

FDA records hold no clearances under product code NXF.

Recent recalls

Product code NXF

FDA records show no recalls under product code NXF.

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)