FDA product code MUR: Graft, Sclera, Reinforcement
MUR is the FDA product code for graft, sclera, reinforcement. It is a Class III device, reviewed by the Ophthalmic panel. Devices under MUR reach the market by Contact FDA; FDA lists no cleared 510(k)s for it.
Classification
| Field | Value |
|---|---|
| Device name | Graft, Sclera, Reinforcement |
| Device class | Class III |
| Review panel | OP — Ophthalmic |
| Medical specialty | Unknown |
| Premarket route | Contact FDA |
| Implant | Yes |
Recalls for MUR devices
openFDA lists no recalls for product code MUR.
Frequently asked questions
What is FDA product code MUR?
MUR is the FDA product code for graft, sclera, reinforcement. It is a Class III device, reviewed by the Ophthalmic panel.
What device class is MUR?
Class III. Typical premarket route: Contact FDA.
Next steps
- Run an FDA pathway report with predicate devices for product code MUR
- Run a recall and safety report across every MUR manufacturer
- Watch product code MUR for new clearances and recalls
Source: openFDA device classification, 510(k), PMA, De Novo and recall data (public domain). Review days run from FDA receipt to decision. Not regulatory advice.