HRSFDA Class 2 · 21 CFR 888.3030 · implantable

Plate, Fixation, Bone

Device family · Orthopedic

Automated profile from regulatory + adverse-event registries · AI-reviewed · expert clinical sign-off in progress — not yet independently verified.
FDA clearances
1,306
Manufacturers
130
Flagged signals
18
Adverse-event reports
34,691

Code matrix

FDA product codeHRS
Device classClass 2
Regulation21 CFR 888.3030
GMDN35359
ImplantableYes
Life-sustainingNo

Adverse-event signals

Public · always free

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

Event typeYearReportsPRRχ²
Other20113399.0827
Other201533332.810,593
Other2012643.4208
Other2010637.3177
Other2010311.219
Other201149.422
Other201597.545
Other201037.010
Other201475.924
Other201354.29
Other201243.44
Injury2011102.614
Injury202382.610
Injury201642.64
Injury202542.64
Injury202442.64
Injury201842.64
Injury2014102.28

Device-level recall linkage pending an FDA-recalls product-code re-ingest. Class 2 family · 34,691 total adverse-event reports.

Manufacturer landscape

ManufacturerClearancesLatestConcern
Synthes (Usa)872011
Wrightmedicaltechnologyinc452021
ARTHREX, INC.392026
Smith & Nephew, Inc.342022
Medartis AG302026
aap Implantate AG252026
Zimmer, Inc.252016
TriMed, Inc.242026
Jeil Medical Corporation242025
NEWCLIP TECHNICS222026
Stryker GmbH212024
Biomet, Inc.202021
Howmedica Corp.201998
DEPUY ORTHOPAEDICS, INC.182012
Howmedica Osteonics Corp.162010
Synthes (USA) Products, LLC152021
In2Bones USA, LLC152024
Onyx Medical Corp.141994
ORTHOPEDIATRICS CORP.122025
KLS-Martin L.P.112026
Skeletal Dynamics, Inc.112026
Biomet Microfixation112024
Tyber Medical, LLC102025
Treace Medical Concepts, Inc.92024
Bonebridge AG92026

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

Recent FDA clearances

I.T.S. PRS Phoenix II · I.T.S. GmbH510(k) · 2026-04-24
POYA 3.5mm Medial Proximal Tibia System · Bonebridge AG510(k) · 2026-04-24
PC Fix System · Chest Wall Innovations, Inc.510(k) · 2026-04-24
SMART Osteotomy System · Actis Medical Pty., Ltd.510(k) · 2026-04-10
enHAnce PEEK Bunion System · Nvision Biomedical Technologies, Inc.510(k) · 2026-04-01
Airlock® Ankle Plating System · Novastep SAS510(k) · 2026-03-25
Vortex5 Tailor's Bunion Correction System · Nvision Biomedical Technologies, Inc.510(k) · 2026-03-25
LOQTEQ® VA Proximal Humerus Plate 3.5 · Aap Implantate AG510(k) · 2026-03-24
Clavicle Fixation System · Skeletal Dynamics, Inc.510(k) · 2026-03-23
CastleLoc Pectus Bar System · L&K BIOMED Co., Ltd.510(k) · 2026-03-19
Super Upper Limbs Versalock Plating System · GM Dos Reis Industria e Comercio Ltda.510(k) · 2026-03-17
APS Spear Locking Plate · A Plus Biotechnology Co., Ltd.510(k) · 2026-03-17
APTUS Shoulder Proximal Humerus System, PentaLock 3.5 · Medartis AG510(k) · 2026-03-16
Xpert Hand · Newclip Technics510(k) · 2026-03-11
DePuy Synthes VOLT™ Proximal Tibia 3.5 Plating System · Synthes GmbH510(k) · 2026-03-09
Arthrex Humeral Plating System (Anatomic Humeral Plate) and Cerclage Button · Arthrex, Inc.510(k) · 2026-03-03
VOLT™ Ankle Trauma 2.7/3.5 Plating System; VOLT™ Calcaneus 2.7 Plating System · Synthes GmbH510(k) · 2026-03-02
HKT Anatomical Locking Trauma System · Hankil Tech Medical Co., Ltd.510(k) · 2026-02-27
RIB LINK™ Fixation System · Globus Medical, Inc.510(k) · 2026-02-26
KLS Martin Ixos System · KLS Martin L.P.510(k) · 2026-02-20
KLS Martin Pure Pectus System · KLS-Martin L.P.510(k) · 2026-02-20
Wrist Fracture System · Met One Technologies, LLC510(k) · 2026-02-12
Arthrex Variable Angle (VA) Proximal Tibia Plating System · Arthrex, Inc.510(k) · 2026-01-21
TriMed Volar Bearing Plates (VBEAL-13-7S); TriMed Volar Bearing Plates (VBEAR-13-7S); TriMed Volar Bearing Plates (VBEAL-14-7S); TriMed Volar Bearing Plates (VBEAR-14-7S); TriMed Volar Bearing Plates (VBEAL-16-7S); TriMed Volar Bearing Plates (VBEAR-16-7S) · TriMed, Inc.510(k) · 2026-01-15
Arthrex Anatomic Lapidus Plates and I-Beam Lapidus Plates · Arthrex, Inc.510(k) · 2026-01-12

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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