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REGENEREX RINGLOC + HIP SYSTEM
Model PT-116044 · Biomet Orthopedics, LLC · DI 00880304460232
JDG — Prosthesis, Hip, Femoral Component, Cemented, Metal · Class II · 21 CFR 888.3360
JDI — Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Cemented · Class II · 21 CFR 888.3350
KWZ — Prosthesis, Hip, Constrained, Cemented Or Uncemented, Metal/Polymer · Class II · 21 CFR 888.3310
LPH — Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Porous Uncemented · Class II · 21 CFR 888.3358
LWJ — Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Uncemented · Class II · 21 CFR 888.3360
LZO — Prosthesis, Hip, Semi-Constrained, Metal/Ceramic/Polymer, Cemented Or Non-Porous, Uncemented · Class II · 21 CFR 888.3353
MAY — Prosthesis, Hip, Semi-Constrained, Metal/Ceramic/Polymer, Cemented Or Non-Porous Cemented, Osteophilic Finish · Class II · 21 CFR 888.3353
MBL — Prosthesis, Hip, Semi-Constrained, Uncemented, Metal/Polymer, Porous · Class II · 21 CFR 888.3358
MEH — Prosthesis, Hip, Semi-Constrained, Uncemented, Metal / Polymer, Non-Porous, Calcium Phosphate · Class II · 21 CFR 888.3353
UDILibrary device dossier · generated 2026-09-07 · 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)
2019-01
0
2.8
2019-02
0
2.4
2019-03
0
2.67
2019-04
0
2.55
2019-05
0
2.06
2019-06
0
1.75
2019-07
0
1.76
2019-08
0
2.03
2019-09
0
2.2
2019-10
0
2.39
2019-11
0
2.04
2019-12
0
2.31
2020-01
0
2.61
2020-02
0
2.39
2020-03
0
3.03
2020-04
0
2.13
2020-05
0
2.18
2020-06
0
2.04
2020-07
0
2.66
2020-08
0
2.29
2020-09
0
2.58
2020-10
0
2.67
2020-11
0
2.55
2020-12
0
2.77
2021-01
0
2.77
2021-02
0
2.24
2021-03
0
2.08
2021-04
0
2.09
2021-05
0
2.33
2021-06
0
2.59
2021-07
0
2.47
2021-08
0
2.4
2021-09
0
2.56
2021-10
0
2.29
2021-11
0
2.2
2021-12
0
2.39
2022-01
0
2.16
2022-02
0
2.28
2022-03
0
2.22
2022-04
0
2.26
2022-05
0
2.2
2022-06
0
2.19
2022-07
0
2.08
2022-08
0
2.14
2022-09
0
2.14
2022-10
0
2.17
2022-11
0
2.17
2022-12
0
2.11
2023-01
0
2.16
2023-02
0
2.06
2023-03
0
2.29
2023-04
0
2.2
2023-05
0
2.16
2023-06
0
2.2
2023-07
0
2.11
2023-08
0
1.98
2023-09
0
1.97
2023-10
0
1.65
2023-11
0
1.63
2023-12
0
1.7
2024-01
0
1.74
2024-02
0
2.02
2024-03
0
1.97
2024-04
0
1.77
2024-05
0
2.13
2024-06
0
1.95
2024-07
0
1.73
2024-08
0
1.95
2024-09
0
2.02
2024-10
0
1.78
2024-11
0
1.71
2024-12
0
1.57
2025-01
0
1.84
2025-02
0
1.52
2025-03
0
1.77
2025-04
0
1.81
2025-05
0
1.68
2025-06
0
1.82
2025-07
0
1.81
2025-08
0
1.68
2025-09
0
1.7
2025-10
0
1.73
2025-11
0
1.76
2025-12
0
1.87
2026-01
0
1.94
2026-02
0
1.63
2026-03
0
1.92
2026-04
0
1.83
2026-05
0
1.7
2026-06
0
1.74
This device (reports/month)Average device in JDG, JDI, KWZ, LPH, LWJ, LZO, MAY, MBL, MEH (reports/device/month)
Regulatory clearances
None linked in the loaded window.
Predicate lineage
K070369 — cited as predicate by K093235, K111863, K112802, K112898, K181491
Lineage extracted from public 510(k) summary text (heuristic).
Manufacturer compliance record — Biomet Orthopedics, LLC