OXGClass II

Mesh, Surgical, Non-Absorbable, Plastic And Reconstructive Surgery

21 CFR 878.3300 / General, Plastic Surgery

OXG is the FDA product code for Mesh, Surgical, Non-Absorbable, Plastic And Reconstructive Surgery, a class II device type, regulated under 21 CFR 878.3300. FDA's definition for this code reads: "For reinforcement of soft tissue where weakness exists in plastic and reconstructive surgery". As of 2026-09-10, FDA records hold no 510(k) clearances under this code and no recalls.

Classification record

Product code: OXG
Device name: Mesh, Surgical, Non-Absorbable, Plastic And Reconstructive Surgery
FDA definition: For reinforcement of soft tissue where weakness exists in plastic and reconstructive surgery.
Regulation: 21 CFR 878.3300
Device class: Class II
Review panel: General, Plastic Surgery
Submission type: 510(k)
Implant: Yes
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

No registered establishment in MDM’s records lists product code OXG.

Recent clearances

Product code OXG

FDA records hold no clearances under product code OXG.

Recent recalls

Product code OXG

FDA records show no recalls under product code OXG.

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)