FDA product code LLP: Laser For Pain Therapy
LLP is the FDA product code for laser for pain therapy. It is a Class III device, reviewed by the Neurology panel. Devices under LLP reach the market by Contact FDA; FDA lists no cleared 510(k)s for it.
Classification
| Field | Value |
|---|---|
| Device name | Laser For Pain Therapy |
| Device class | Class III |
| Review panel | NE — Neurology |
| Medical specialty | Unknown |
| Premarket route | Contact FDA |
Recalls for LLP devices
openFDA lists no recalls for product code LLP.
Frequently asked questions
What is FDA product code LLP?
LLP is the FDA product code for laser for pain therapy. It is a Class III device, reviewed by the Neurology panel.
What device class is LLP?
Class III. Typical premarket route: Contact FDA.
Next steps
- Run an FDA pathway report with predicate devices for product code LLP
- Run a recall and safety report across every LLP manufacturer
- Watch product code LLP 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.