FDA product code MOZ: Acid, Hyaluronic, Intraarticular
MOZ is the FDA product code for acid, hyaluronic, intraarticular. It is a Class III device, reviewed by the Orthopedic panel. Devices under MOZ reach the market by PMA; FDA lists no cleared 510(k)s for it. 14 PMA applications cite this product code. FDA has posted 2 recalls for MOZ devices.
Classification
| Field | Value |
|---|---|
| Device name | Acid, Hyaluronic, Intraarticular |
| Device class | Class III |
| Review panel | OR — Orthopedic |
| Medical specialty | Unknown |
| Premarket route | PMA |
Recalls for MOZ devices
2 product recalls in 2 recall events; 0 initiated in the last five years and 0 still open. Most recent: 2017-12-11.
| Year | Recalls |
|---|---|
| 2017 | 1 |
Frequently asked questions
What is FDA product code MOZ?
MOZ is the FDA product code for acid, hyaluronic, intraarticular. It is a Class III device, reviewed by the Orthopedic panel.
What device class is MOZ?
Class III. Typical premarket route: PMA.
Have MOZ devices been recalled?
Yes: 2 product recalls across 2 recall events; the most recent began 2017-12-11.
Next steps
- Run an FDA pathway report with predicate devices for product code MOZ
- Run a recall and safety report across every MOZ manufacturer
- Watch product code MOZ 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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