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MAESTRO TOTAL WRIST
Model 180423 · Biomet Orthopedics, LLC · DI 00880304555143
JWJ — Prosthesis, Wrist, 3 Part Metal-Plastic-Metal Articulation, Semi-Constrained · Class II · 21 CFR 888.3800
UDILibrary device dossier · generated 2026-09-12 · sources: FDA GUDID, openFDA (recalls, MAUDE, 510(k)/PMA), FDA Data Dashboard (inspections, compliance actions), 510(k) summary documents.
Recall history (0)
No recalls linked in the loaded window.
Adverse-event reports — MAUDE (0)
Caveat (required reading): 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 is a reporting baseline (average device in the same product code), not a risk measure.
Monthly adverse-event reports for this device versus the product-code average.
Month
This device (reports)
Product-code average (reports per device)
2019-07
0
1
2019-09
0
1
2019-11
0
1
2021-02
0
1
2021-09
0
1
2022-05
0
1.5
2022-11
0
1.5
2022-12
0
2
2023-10
0
1
2023-11
0
1
2023-12
0
1
2024-01
0
1
2024-10
0
1
2025-02
0
1
2025-05
0
1
2025-06
0
2
2025-09
0
1
2026-05
0
1
This device (reports/month)Average device in JWJ (reports/device/month)
Regulatory clearances
None linked in the loaded window.
Manufacturer compliance record — Biomet Orthopedics, LLC