MICROPORT ORTHOPEDICS INC.

Manufacturer adverse-event records for MICROPORT ORTHOPEDICS INC. come from the U.S. Food & Drug Administration (FDA) MAUDE database via openFDA, refreshed March 2026 - see our methodology. Not medical advice.

FDA MAUDE device safety record · 2012–2026 · mid-book · typical Death-code · injury-heavy

Injury-mix signature

MICROPORT ORTHOPEDICS INC. leans injury-heavy in event_type mix

Injury-coded event_type share is 98.7% (injury-heavy tercile) beside 0.11% Death-coded (typical). Volume band: mid.

What the Injury-mix reading shows for MICROPORT ORTHOPEDICS INC.

The standout signal for MICROPORT ORTHOPEDICS INC. is Injury-mix: 98.7% Injury-coded (injury-heavy) beside 0.11% Death-coded, on a mid-book footprint.

Mid-pack volume still shows a clear device fingerprint; the table below is the actionable layer for MICROPORT ORTHOPEDICS INC.. Event_type Death/Injury codes differ from patient-outcome rows - see methodology.

Reports span 20 device types, led in this extract by Injury at 12,677 (98.7% of event_type total). Peak single-year volume reaches 2,075 reports across 14 years. These are raw FDA submissions, not adjudicated findings. Snapshot . Verify current communications on the FDA MDR page.

12,839
Total Reports
14
Event-type Death
12,677
Injury Reports
20
Device Types

Event Types

Injury 12,677 (98.7%)
Malfunction 104 (0.8%)
43 (0.3%)
Death 14 (0.1%)
Other 1 (0.0%)

Patient Outcomes

FDA patient-outcome codes (separate from event_type). Percentages use this chart's row total.

Required Intervention 12,445 (96.6%)
186 (1.4%)
Other 134 (1.0%)
R 66 (0.5%)
Hospitalization 30 (0.2%)
Death 18 (0.1%)
O 4 (0.0%)
Disability 1 (0.0%)

Yearly Trend

12
2012: 1
14
2014: 1,845
15
2015: 2,075
16
2016: 1,548
17
2017: 1,603
18
2018: 1,557
19
2019: 1,162
20
2020: 825
21
2021: 611
22
2022: 455
23
2023: 241
24
2024: 501
25
2025: 383
26
2026: 32