FDA product code LMN: Ceramics, Calcium Triphosphate/Hydroxypatite, Non-Load Bearing Uses
LMN is the FDA product code for ceramics, calcium triphosphate/hydroxypatite, non-load bearing uses. It is a Class III device, reviewed by the Orthopedic panel. Devices under LMN reach the market by PMA; FDA lists no cleared 510(k)s for it. 1 PMA application cites this product code.
Classification
| Field | Value |
|---|---|
| Device name | Ceramics, Calcium Triphosphate/Hydroxypatite, Non-Load Bearing Uses |
| Device class | Class III |
| Review panel | OR — Orthopedic |
| Medical specialty | Unknown |
| Premarket route | PMA |
Recalls for LMN devices
openFDA lists no recalls for product code LMN.
Frequently asked questions
What is FDA product code LMN?
LMN is the FDA product code for ceramics, calcium triphosphate/hydroxypatite, non-load bearing uses. It is a Class III device, reviewed by the Orthopedic panel.
What device class is LMN?
Class III. Typical premarket route: PMA.
Next steps
- Run an FDA pathway report with predicate devices for product code LMN
- Run a recall and safety report across every LMN manufacturer
- Watch product code LMN 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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