JDIFDA Class 2 · 21 CFR 888.3350 · implantable

Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Cemented

Device family · Orthopedic

Automated profile from regulatory + adverse-event registries · AI-reviewed · expert clinical sign-off in progress — not yet independently verified.
FDA clearances
562
Manufacturers
51
Flagged signals
12
Adverse-event reports
64,376

Code matrix

FDA product codeJDI
Device classClass 2
Regulation21 CFR 888.3350
GMDN— (crosswalk pending)
ImplantableYes
Life-sustainingNo

Adverse-event signals

Public · always free

MAUDE disproportionality (PRR), flagged where PRR ≥ 2, χ² ≥ 4, count ≥ 3.

Event typeYearReportsPRRχ²
Other20104895.74,404
Other2011353.9108
Other20112549.81,148
Other20131937.8646
Other20121529.9391
Other201036.08
Other2014123.115
Other201092.78
Other2012102.68
Other2015102.68
Injury202372.04
Injury201372.04

Device-level recall linkage pending an FDA-recalls product-code re-ingest. Class 2 family · 64,376 total adverse-event reports.

Manufacturer landscape

ManufacturerClearancesLatestConcern
Biomet, Inc.502015
Depuy, Inc.451998
Howmedica Corp.351998
Osteonics Corp.291998
Zimmer, Inc.272021
Intermedics Orthopedics211997
Kirschner Medical Corp.171994
Howmedica Osteonics Corp.162020
Orthomet, Inc.161994
Encore Orthopedics, Inc.131999
Exactech, Inc.122005
DEPUY ORTHOPAEDICS, INC.122009
Wrightmedicaltechnologyinc112004
Implex Corp.102000
Johnson & Johnson Professionals, Inc.91998
Smith & Nephew, Inc.82024
Richards Medical Co., Inc.71988
Orthopedic Systems, Inc.71991
BIOPRO, INC.72009
Richard'S Medical Equip., Inc.71983
Smith & Nephew Richards, Inc.71996
Dow Corning Wright51991
Stelkast Company51999
Corin USA42015
Kinamed, Inc.31995

Concern score lights up where a maker maps to a scored entity (depth fast-follow).

Recent FDA clearances

Trabecular Metal Acetabular Revision System, Acetabular Liners and Constrained Liners · Zimmer Biomet510(k) · 2025-07-31
Anthology Hip Stems; CPCS Hip Stems; Femoral Heads; R3 Acetabular Liners; Spectron Hip Stems; Synergy Hip Stems · Smith & Nephew, Inc.510(k) · 2024-10-21
Global Modular Replacement System, Modular Replacement System, Modular Rotating Hinge Knee Component · Howmedica Osteonics Corp., Dba Stryker Orthopaedics510(k) · 2024-08-02
Stryker Orthopaedics Hip Systems Labeling Update · Howmedica Osteonics Corp., Dba Stryker Orthopaedics510(k) · 2024-04-12
Global Modular Replacement System · Howmedica Osteonics Corp. A.K.A. Stryker Orthopaedics510(k) · 2023-12-08
Global Modular Replacement System, Modular Replacement System, Modular Rotating Hinge Knee · Howmedica Osteonics Corp., Dba Stryker Orthopaedics510(k) · 2023-01-26
C-Stem AMT LE Prosthesis · Depuy Ireland UC510(k) · 2022-07-22
Exeter® X3® RimFit® Cup · Howmedica Osteonics Corp., Dba Stryker Orthopaedics510(k) · 2022-02-01
MPO Hip Instruments · Microport Orthopedics, Inc.510(k) · 2022-01-05
VerSys Cemented Revision/Calcar · Zimmer, Inc.510(k) · 2021-12-10
ELEOS Limb Salvage System with BioGrip · Onkos Surgical510(k) · 2021-06-09
ELEOS™ Limb Salvage System · Onkos Surgical510(k) · 2021-02-05
ELEOS Limb Salvage System featuring BIOGRIP · Onkos Surgical510(k) · 2020-12-11
PROFEMUR® GLADIATOR® Cemented Classic Stem · Microport Orthopedics, Inc.510(k) · 2020-12-10
Exeter V40 Femoral Stem, Exeter X3 RimFit Cup · Howmedica Osteonics Corp.510(k) · 2020-08-13
ZCA All-Poly Acetabular Cups · Zimmer, Inc.510(k) · 2020-07-16
Zimmer, Inc. Hip Joint Prostheses MR Labeling I · Zimmer, Inc.510(k) · 2020-07-09
CPT Hip System · Zimmer, Inc.510(k) · 2020-03-20
Conformity stem, cemented · United Orthopedic Corporation510(k) · 2020-01-03
EXETER Centralizer, EXETER 2.5mm Plug · Stryker Orthopaedics510(k) · 2019-08-28
Cemented TSI Hip Stem · Signature Orthopaedics Pty, Ltd.510(k) · 2019-02-11
Libertas Hip Replacement System · Maxx Orthopedics, Inc.510(k) · 2018-09-28
MALUC™ Total Hip Arthroplasty System · Surgtech, Inc.510(k) · 2017-05-10
REDAPT Anteverted Cemented Liner · Smith & Nephew, Inc.510(k) · 2016-11-17
FitRite™ Total Hip Arthroplasty System · Excera Orthopedics, Inc.510(k) · 2016-06-23

Sources: FDA 510(k)/PMA · openFDA MAUDE · FDA device classification · MedevIQ manufacturer-canonical. Registry data, AI-reviewed; expert clinical sign-off in progress.

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