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) |
|---|---|---|
| 2019-01 | 0 | 2.08 |
| 2019-02 | 0 | 1.98 |
| 2019-03 | 0 | 1.65 |
| 2019-04 | 0 | 1.96 |
| 2019-05 | 0 | 1.8 |
| 2019-06 | 0 | 2.06 |
| 2019-07 | 0 | 2 |
| 2019-08 | 0 | 2.18 |
| 2019-09 | 0 | 1.89 |
| 2019-10 | 0 | 2.21 |
| 2019-11 | 0 | 2.83 |
| 2019-12 | 0 | 2.3 |
| 2020-01 | 0 | 2.25 |
| 2020-02 | 0 | 2.6 |
| 2020-03 | 0 | 2.17 |
| 2020-04 | 0 | 2.01 |
| 2020-05 | 0 | 1.72 |
| 2020-06 | 0 | 2.02 |
| 2020-07 | 0 | 2.49 |
| 2020-08 | 0 | 2.59 |
| 2020-09 | 0 | 2.13 |
| 2020-10 | 0 | 2.66 |
| 2020-11 | 0 | 2.67 |
| 2020-12 | 0 | 2.67 |
| 2021-01 | 0 | 2.26 |
| 2021-02 | 0 | 2.25 |
| 2021-03 | 0 | 2.39 |
| 2021-04 | 0 | 2.26 |
| 2021-05 | 0 | 2.18 |
| 2021-06 | 0 | 2.12 |
| 2021-07 | 0 | 2.16 |
| 2021-08 | 0 | 1.82 |
| 2021-09 | 0 | 2.23 |
| 2021-10 | 0 | 1.9 |
| 2021-11 | 0 | 2.16 |
| 2021-12 | 0 | 2.25 |
| 2022-01 | 0 | 1.89 |
| 2022-02 | 0 | 2.24 |
| 2022-03 | 0 | 1.92 |
| 2022-04 | 0 | 1.99 |
| 2022-05 | 0 | 2.2 |
| 2022-06 | 0 | 1.92 |
| 2022-07 | 0 | 1.98 |
| 2022-08 | 0 | 1.96 |
| 2022-09 | 0 | 2.32 |
| 2022-10 | 0 | 2.06 |
| 2022-11 | 0 | 2.11 |
| 2022-12 | 0 | 1.77 |
| 2023-01 | 0 | 1.94 |
| 2023-02 | 0 | 2.07 |
| 2023-03 | 0 | 2.07 |
| 2023-04 | 0 | 2.09 |
| 2023-05 | 0 | 2.24 |
| 2023-06 | 0 | 2.15 |
| 2023-07 | 0 | 1.88 |
| 2023-08 | 0 | 1.62 |
| 2023-09 | 0 | 1.63 |
| 2023-10 | 0 | 1.54 |
| 2023-11 | 0 | 1.62 |
| 2023-12 | 0 | 1.59 |
| 2024-01 | 0 | 1.51 |
| 2024-02 | 0 | 1.63 |
| 2024-03 | 0 | 1.68 |
| 2024-04 | 0 | 1.57 |
| 2024-05 | 0 | 1.76 |
| 2024-06 | 0 | 1.83 |
| 2024-07 | 0 | 1.71 |
| 2024-08 | 1 | 2.13 |
| 2024-09 | 0 | 1.85 |
| 2024-10 | 0 | 1.85 |
| 2024-11 | 0 | 1.8 |
| 2024-12 | 0 | 1.93 |
| 2025-01 | 0 | 2.12 |
| 2025-02 | 0 | 1.7 |
| 2025-03 | 0 | 1.69 |
| 2025-04 | 0 | 1.56 |
| 2025-05 | 0 | 1.61 |
| 2025-06 | 0 | 1.68 |
| 2025-07 | 0 | 1.56 |
| 2025-08 | 0 | 1.57 |
| 2025-09 | 0 | 1.53 |
| 2025-10 | 0 | 1.4 |
| 2025-11 | 0 | 1.58 |
| 2025-12 | 1 | 1.57 |
| 2026-01 | 0 | 1.48 |
| 2026-02 | 0 | 1.47 |
| 2026-03 | 0 | 1.82 |
| 2026-04 | 0 | 1.62 |
| 2026-05 | 0 | 1.61 |
| 2026-06 | 0 | 1.58 |
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 |
|---|---|---|---|---|
| 2025-12-09 | 3010266064-2025-00260 | Malfunction | Available | exact di |
| 2024-08-22 | 3010266064-2024-00172 | Malfunction | Available | exact di |
Regulatory clearances
- 510(k)K240113Substantially equivalent (SESE) · 2024-03-18clearance family
Predicate lineage
- K240113
- K073325
- K091543
- K093746
- K100897
- K102069
- K111711
- K121443
- K141471
- K142807
- K152726
- K180334
- K190085
- K191211
- K210566
- K211221
- K211512
- K221224
- K240139
- K951987
- K962557
Cited as predicate by: K242272
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 |
|---|---|---|---|---|
| 2025-01-27 | NAI | No action indicated | Integrity Orthopaedics Inc | 0 |
| 2023-05-03 | NAI | No action indicated | CARTIHEAL, LTD | 0 |
| 2021-12-09 | VAI | Voluntary action indicated | Smith & Nephew, Inc. | 1 |
| 2021-12-09 | VAI | Voluntary action indicated | Smith & Nephew, Inc. | 1 |
| 2021-10-26 | NAI | No action indicated | Smith & Nephew Inc. | 0 |
| 2021-10-26 | NAI | No action indicated | Smith & Nephew Inc. | 0 |
| 2020-02-06 | VAI | Voluntary action indicated | Blue Belt Technologies, Inc | 6 |
| 2019-10-25 | NAI | No action indicated | Tusker Medical, Inc. | 0 |
| 2019-10-08 | VAI | Voluntary action indicated | Tusker Medical, Inc. | 3 |
| 2018-03-30 | NAI | No action indicated | Ascension Orthopedics, Inc | 0 |
| 2018-02-02 | NAI | No action indicated | Smith & Nephew, Inc. | 0 |
| 2018-02-02 | NAI | No action indicated | Smith & Nephew, Inc. | 0 |
| 2018-01-30 | NAI | No action indicated | Smith & Nephew | 0 |
| 2017-08-21 | NAI | No action indicated | Smith & Nephew, Inc. Advanced Surgical Devices Division | 0 |
| 2017-08-02 | VAI | Voluntary action indicated | Smith & Nephew, Inc. | 3 |
| 2017-08-02 | VAI | Voluntary action indicated | Smith & Nephew, Inc. | 3 |
| 2017-07-24 | NAI | No action indicated | Smith & Nephew, Inc. | 0 |
| 2017-07-24 | NAI | No action indicated | Smith & Nephew, Inc. | 0 |
| 2017-05-25 | NAI | No action indicated | Smith & Nephew, Inc. | 0 |
| 2017-05-25 | NAI | No action indicated | Smith & Nephew, Inc. | 0 |
| 2015-04-30 | WL | Warning Letter | Smith & Nephew Inc. | — |
| 2015-04-30 | WL | Warning Letter | Smith & Nephew Inc. | — |
| 2014-06-11 | WL | Warning Letter | Smith & Nephew, Inc. | — |
| 2010-09-16 | WL | Warning Letter | Ascension Orthopedics, Inc | — |
Similar devices
- EXULT Knee Replacement System Corentec Co., Ltd
- 'VANGUARD(TM) Biomet Orthopedics, LLC
- 'VANGUARD(TM) Biomet Orthopedics, LLC
- 'VANGUARD(TM) Biomet Orthopedics, LLC
- 'VANGUARD(TM) Biomet Orthopedics, LLC
- 'VANGUARD(TM) Biomet Orthopedics, LLC
- 'VANGUARD(TM) Biomet Orthopedics, LLC
- 'VANGUARD(TM) Biomet Orthopedics, LLC
- 'VANGUARD(TM) Biomet Orthopedics, LLC
- 'VANGUARD(TM) Biomet Orthopedics, LLC
- 'VANGUARD(TM) Biomet Orthopedics, LLC
- 'VANGUARD(TM) Biomet Orthopedics, LLC
Select up to two to place side-by-side with this device.