FDA product code REA: High-Power Laser Light Show Projector
REA is the FDA product code for high-power laser light show projector. It is a Not classified device, reviewed by the Unknown panel. FDA has posted 12 recalls for REA devices, 4 initiated in the last five years.
Definition
Product, laser, demo, projector, laser light show/display, class iiib/iv/3b/4; Laser projection system that incorporates a laser having a maximum radiation output power greater than 5mw.
Classification
| Field | Value |
|---|---|
| Device name | High-Power Laser Light Show Projector |
| Device class | Not classified |
| Medical specialty | Unknown |
| GMP exempt | Yes |
Recalls for REA devices
12 product recalls in 6 recall events; 4 initiated in the last five years and 9 still open. Most recent: 2025-06-30.
| Year | Recalls |
|---|---|
| 2017 | 1 |
| 2019 | 5 |
| 2022 | 1 |
| 2025 | 3 |
Frequently asked questions
What is FDA product code REA?
REA is the FDA product code for high-power laser light show projector. It is a Not classified device, reviewed by the Unknown panel.
What device class is REA?
Not classified.
Have REA devices been recalled?
Yes: 12 product recalls across 6 recall events; the most recent began 2025-06-30.
Next steps
- Run an FDA pathway report with predicate devices for product code REA
- Run a recall and safety report across every REA manufacturer
- Watch product code REA 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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