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 reportsMalfunction 2
| Month | This device (reports) | Product-code average (reports per device) |
|---|---|---|
| 2021-07 | 0 | 1 |
| 2023-10 | 2 | 3 |
| 2023-11 | 0 | 1 |
| 2024-03 | 0 | 2 |
| 2026-01 | 0 | 2.5 |
| 2026-03 | 0 | 7 |
| 2026-04 | 0 | 1.5 |
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 |
|---|---|---|---|---|
| 2023-10-30 | 2518422-2023-27990 | Malfunction | Available | procode brand trgm |
| 2023-10-10 | 2518422-2023-25729 | Malfunction | Available | procode brand trgm |
Regulatory clearances
None linked.
Manufacturer compliance record
| Date | Type | Outcome | Facility | Citations |
|---|---|---|---|---|
| 2023-02-14 | OAI | Official action indicated | Respironics, Inc. | 1 |
| 2016-12-07 | NAI | No action indicated | Respironics, Inc. | 0 |
| 2015-01-28 | NAI | No action indicated | Respironics, Inc. | 0 |
| 2012-06-15 | NAI | No action indicated | Respironics, Inc. | 0 |
| 2010-09-01 | NAI | No action indicated | Respironics, Inc. | 0 |
| 2010-06-22 | NAI | No action indicated | Respironics, Inc. | 0 |
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