FDA product code LTG: Paste, Injectable For Vocal Cord Augmentation
LTG is the FDA product code for paste, injectable for vocal cord augmentation. It is a Class III device, reviewed by the Dental panel. Devices under LTG 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 | Paste, Injectable For Vocal Cord Augmentation |
| Device class | Class III |
| Review panel | DE — Dental |
| Medical specialty | Unknown |
| Premarket route | PMA |
Recalls for LTG devices
openFDA lists no recalls for product code LTG.
Frequently asked questions
What is FDA product code LTG?
LTG is the FDA product code for paste, injectable for vocal cord augmentation. It is a Class III device, reviewed by the Dental panel.
What device class is LTG?
Class III. Typical premarket route: PMA.
Next steps
- Run an FDA pathway report with predicate devices for product code LTG
- Run a recall and safety report across every LTG manufacturer
- Watch product code LTG 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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