OVCNot classified

Headframe

Unknown

OVC is the FDA product code for Headframe. FDA's definition for this code reads: "To enhance mechanical thrombus dissolution and acceleration of thrombolysis in patients suffering acute ischemic stroke". As of 2026-09-10, FDA records hold no 510(k) clearances under this code and no recalls.

Classification record

Product code: OVC
Device name: Headframe
FDA definition: To enhance mechanical thrombus dissolution and acceleration of thrombolysis in patients suffering acute ischemic stroke.
Device class: Not classified
Review panel: Unknown
Submission type: Contact ODE
Implant: No
Life sustaining or supporting: No
GMP exempt: Yes
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 OVC.

Recent clearances

Product code OVC

FDA records hold no clearances under product code OVC.

Recent recalls

Product code OVC

FDA records show no recalls under product code OVC.

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)