Adverse-event reports (MAUDE)
Read this first: MAUDE report counts cannot be used to compute incidence rates or compare device safety. Reporting is incomplete, duplicated, and spikes with publicity; there is no denominator of devices in use. The peer line shows reporting volume for the average device in the same FDA product code — a reporting baseline, not a risk measure.
2 linked reportsInjury 2
| Month | This device (reports) | Product-code average (reports per device) |
|---|---|---|
| 2019-01 | 0 | 1.5 |
| 2019-02 | 0 | 1.33 |
| 2019-03 | 0 | 1.33 |
| 2019-04 | 0 | 1.5 |
| 2019-07 | 0 | 1 |
| 2019-08 | 0 | 1.25 |
| 2019-09 | 0 | 2 |
| 2019-10 | 0 | 1 |
| 2019-11 | 0 | 1 |
| 2019-12 | 0 | 2 |
| 2020-01 | 0 | 1 |
| 2020-02 | 0 | 1 |
| 2020-04 | 0 | 1 |
| 2020-08 | 0 | 1.25 |
| 2020-09 | 0 | 4.5 |
| 2020-11 | 0 | 2 |
| 2020-12 | 0 | 1.6 |
| 2021-03 | 0 | 1 |
| 2021-04 | 0 | 1.5 |
| 2021-05 | 2 | 2 |
| 2021-07 | 0 | 4.5 |
| 2021-08 | 0 | 4.67 |
| 2021-09 | 0 | 1 |
| 2021-10 | 0 | 1 |
| 2021-11 | 0 | 1 |
| 2021-12 | 0 | 1.5 |
| 2022-01 | 0 | 2 |
| 2022-02 | 0 | 2.5 |
| 2022-03 | 0 | 1 |
| 2022-04 | 0 | 1.5 |
| 2022-05 | 0 | 1.67 |
| 2022-06 | 0 | 2.5 |
| 2022-07 | 0 | 2.2 |
| 2022-08 | 0 | 2.25 |
| 2022-09 | 0 | 1 |
| 2022-10 | 0 | 2.25 |
| 2022-11 | 0 | 1.75 |
| 2022-12 | 0 | 1 |
| 2023-01 | 0 | 1 |
| 2023-03 | 0 | 1.33 |
| 2023-04 | 0 | 1 |
| 2023-08 | 0 | 4 |
| 2023-11 | 0 | 5 |
| 2023-12 | 0 | 1.33 |
| 2024-01 | 0 | 1 |
| 2024-03 | 0 | 1.33 |
| 2024-04 | 0 | 1 |
| 2024-06 | 0 | 1.5 |
| 2024-07 | 0 | 1 |
| 2024-09 | 0 | 1 |
| 2024-10 | 0 | 1 |
| 2024-11 | 0 | 1 |
| 2025-01 | 0 | 1.67 |
| 2025-03 | 0 | 2 |
| 2025-05 | 0 | 1 |
| 2025-06 | 0 | 1.5 |
| 2025-08 | 0 | 1 |
Failure-mode summaryAI-generated
2 linked report narratives available — no AI summary generated yet.
Recall history
No recalls linked.
Individual MAUDE reports
| Date | Report # | Type | Narrative | Link basis |
|---|---|---|---|---|
| 2021-05-14 | 3004450661-2021-00005 | Injury | Available | catalog number |
Showing the most recent 1 of 2 linked reports.
Regulatory clearances
- 510(k)K171242Substantially equivalent (SESE) · 2017-07-14clearance family
Predicate lineage
Lineage each submission cites, walked transitively (indented = the cited device's own predicates). Extracted from public 510(k) summary text — heuristic, and includes reference devices mentioned alongside true predicates.
Manufacturer compliance record
| Date | Type | Outcome | Facility | Citations |
|---|---|---|---|---|
| 2013-12-11 | NAI | No action indicated | Alma Lasers, Inc. | 0 |
| 2013-12-11 | NAI | No action indicated | Alma Lasers, Inc. | 0 |
| 2013-06-07 | WL | Warning Letter | Alma Lasers, Inc. | — |
| 2013-06-07 | WL | Warning Letter | Alma Lasers, Inc. | — |
| 2013-01-29 | OAI | Official action indicated | Alma Lasers, Inc. | 0 |
| 2013-01-29 | OAI | Official action indicated | Alma Lasers, Inc. | 0 |
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