FDA product code LXU: Laser For Wound Healing
LXU is the FDA product code for laser for wound healing. It is a Class III device, reviewed by the General and Plastic Surgery panel. Devices under LXU reach the market by Contact FDA; FDA lists no cleared 510(k)s for it.
Classification
| Field | Value |
|---|---|
| Device name | Laser For Wound Healing |
| Device class | Class III |
| Review panel | SU — General and Plastic Surgery |
| Medical specialty | Unknown |
| Premarket route | Contact FDA |
Recalls for LXU devices
openFDA lists no recalls for product code LXU.
HCPCS codes with matching descriptors
Text match between the FDA device name and CMS descriptors, not an official crosswalk:
- S9055 — Procuren or other growth factor preparation to promote wound healing
Frequently asked questions
What is FDA product code LXU?
LXU is the FDA product code for laser for wound healing. It is a Class III device, reviewed by the General and Plastic Surgery panel.
What device class is LXU?
Class III. Typical premarket route: Contact FDA.
Next steps
- Run an FDA pathway report with predicate devices for product code LXU
- Run a recall and safety report across every LXU manufacturer
- Watch product code LXU 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.
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