FDA product code RIM: Laser Marker, Cutter, Or Engraver, Tabletop, Consumer
RIM is the FDA product code for laser marker, cutter, or engraver, tabletop, consumer. It is a Not classified device, reviewed by the Unknown panel. FDA has posted 1 recall for RIM devices, 1 initiated in the last five years.
Definition
A laser intended for consumer, non-industrial, applications to mark, cut, or engrave objects with text, logos, etc. using either a mask or a scanned laser beam in a portable/tabletop/desktop size, often marketed as do it yourself (DIY) tools.
Classification
| Field | Value |
|---|---|
| Device name | Laser Marker, Cutter, Or Engraver, Tabletop, Consumer |
| Device class | Not classified |
| Medical specialty | Unknown |
| GMP exempt | Yes |
Recalls for RIM devices
1 product recalls in 1 recall events; 1 initiated in the last five years and 1 still open. Most recent: 2024-06-07.
| Year | Recalls |
|---|---|
| 2024 | 1 |
Frequently asked questions
What is FDA product code RIM?
RIM is the FDA product code for laser marker, cutter, or engraver, tabletop, consumer. It is a Not classified device, reviewed by the Unknown panel.
What device class is RIM?
Not classified.
Have RIM devices been recalled?
Yes: 1 product recalls across 1 recall events; the most recent began 2024-06-07.
Next steps
- Run an FDA pathway report with predicate devices for product code RIM
- Run a recall and safety report across every RIM manufacturer
- Watch product code RIM 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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