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.
| Month | This device (reports) | Product-code average (reports per device) |
|---|---|---|
| 2019-07 | 0 | 1 |
| 2021-02 | 0 | 7 |
| 2023-03 | 0 | 1 |
| 2024-06 | 0 | 2 |
| 2024-11 | 0 | 1 |
| 2025-10 | 0 | 2 |
| 2026-03 | 3 | 3 |
3 linked report narratives available — no AI summary generated yet.
No recalls linked.
| Date | Report # | Type | Narrative | Link basis |
|---|---|---|---|---|
| 2026-03-20 | 3004973408-2026-00001 | Injury | Available | catalog number |
Showing the most recent 1 of 3 linked reports.
Predicate lineage
Cited as predicate by: K151029, K182479, K190315, K191510, K200279, K200825, K212181, K220162, K242531, K252493, K252775, K260059, K260280, K260591, K261027
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.
| Date | Type | Outcome | Facility | Citations |
|---|---|---|---|---|
| 2013-11-21 | NAI | No action indicated | Phadia GmbH | 0 |
| 2011-08-18 | NAI | No action indicated | Phadia Ab | 0 |
| 2011-08-18 | NAI | No action indicated | Phadia Ab | 0 |
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