FDA product code REU: Laser Aiming Product, Visible
REU is the FDA product code for laser aiming product, visible. It is a Not classified device, reviewed by the Unknown panel. FDA has posted 2 recalls for REU devices, 1 initiated in the last five years.
Definition
Product, laser, aiming, visible, attached to weapon; An optical devices, using a visible beam of laser light that permits the alignment of a gun, cannon or rocket system with its target
Classification
| Field | Value |
|---|---|
| Device name | Laser Aiming Product, Visible |
| Device class | Not classified |
| Medical specialty | Unknown |
| GMP exempt | Yes |
Recalls for REU devices
2 product recalls in 2 recall events; 1 initiated in the last five years and 1 still open. Most recent: 2026-04-06.
| Year | Recalls |
|---|---|
| 2017 | 1 |
| 2026 | 1 |
Frequently asked questions
What is FDA product code REU?
REU is the FDA product code for laser aiming product, visible. It is a Not classified device, reviewed by the Unknown panel.
What device class is REU?
Not classified.
Have REU devices been recalled?
Yes: 2 product recalls across 2 recall events; the most recent began 2026-04-06.
Next steps
- Run an FDA pathway report with predicate devices for product code REU
- Run a recall and safety report across every REU manufacturer
- Watch product code REU 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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