FDA product code REP: Surveying Laser Product
REP is the FDA product code for surveying laser product. It is a Not classified device, reviewed by the Unknown panel. FDA has posted 4 recalls for REP devices, 1 initiated in the last five years.
Definition
Product, laser, surveying, instrument, determine position by measurement of angles
Classification
| Field | Value |
|---|---|
| Device name | Surveying Laser Product |
| Device class | Not classified |
| Medical specialty | Unknown |
| GMP exempt | Yes |
Recalls for REP devices
4 product recalls in 4 recall events; 1 initiated in the last five years and 2 still open. Most recent: 2025-03-26.
| Year | Recalls |
|---|---|
| 2018 | 1 |
| 2021 | 1 |
| 2025 | 1 |
Frequently asked questions
What is FDA product code REP?
REP is the FDA product code for surveying laser product. It is a Not classified device, reviewed by the Unknown panel.
What device class is REP?
Not classified.
Have REP devices been recalled?
Yes: 4 product recalls across 4 recall events; the most recent began 2025-03-26.
Next steps
- Run an FDA pathway report with predicate devices for product code REP
- Run a recall and safety report across every REP manufacturer
- Watch product code REP 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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