FDA product code RET: Laser Target Designator
RET is the FDA product code for laser target designator. It is a Not classified device, reviewed by the Unknown panel. FDA has posted 3 recalls for RET devices.
Definition
Product, laser, target designator; An optical devices, using a beam of laser radiation that permits the alignment of a firearm-type product such as a gun, cannon, or rocket system with its target.
Classification
| Field | Value |
|---|---|
| Device name | Laser Target Designator |
| Device class | Not classified |
| Medical specialty | Unknown |
| GMP exempt | Yes |
Recalls for RET devices
3 product recalls in 2 recall events; 0 initiated in the last five years and 2 still open. Most recent: 2019-01-29.
| Year | Recalls |
|---|---|
| 2019 | 2 |
Frequently asked questions
What is FDA product code RET?
RET is the FDA product code for laser target designator. It is a Not classified device, reviewed by the Unknown panel.
What device class is RET?
Not classified.
Have RET devices been recalled?
Yes: 3 product recalls across 2 recall events; the most recent began 2019-01-29.
Next steps
- Run an FDA pathway report with predicate devices for product code RET
- Run a recall and safety report across every RET manufacturer
- Watch product code RET 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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