DZEFDA Class 2 · 21 CFR 872.3640 · implantable

Implant, Endosseous, Root-Form

Device family · Dental

Automated profile from regulatory + adverse-event registries · AI-reviewed · expert clinical sign-off in progress — not yet independently verified.
FDA clearances
1,551
Manufacturers
105
Flagged signals
20
Adverse-event reports
3,527,072

Code matrix

FDA product codeDZE
Device classClass 2
Regulation21 CFR 872.3640
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
Other20133665.01,382
Other2012641.1197
Other2011534.3130
Other2010320.638
Other2024319.235
Other202537.912
Injury202042.64
Injury20192522.6404
Injury202352.66
Injury201442.64
Injury2023282.643
Injury2018242.636
Injury202342.64
Injury20241112.4141
Injury202272.36
Injury2023182.218
Injury20252442.2266
Injury2010112.210
Injury2019402.137
Injury2019202.015

Device-level recall linkage pending an FDA-recalls product-code re-ingest. Class 2 family · 3,527,072 total adverse-event reports.

Manufacturer landscape

ManufacturerClearancesLatestConcern
Nobelpharma USA, Inc.511996
Steri-Oss, Inc.401998
Implant Innovations, Inc.372007
Nobel Biocare AB302026
Institut Straumann AG302026
OSSTEM IMPLANT Co., Ltd.272023
BioHorizons Implant Systems, Inc.262024
Lifecore Biomedical, Inc.232007
Straumann USA192016
Zimmer Dental, Inc.192017
DENTIS CO., LTD.192026
MegaGen Implant Co., Ltd.162024
HIOSSEN, INC.152024
Interpore Intl.121996
KJ MEDITECH Co., Ltd.102022
Cowellmedi Co., Ltd.92024
Dentium Co., Ltd.92022
ACE SURGICAL SUPPLY CO., INC.92010
Thommen Medical AG92017
Blue Sky Bio, LLC82022
Z-Systems AG82020
curasan AG82001
ARUM DENTISTRY Co., Ltd.72025
DIO Corporation72018
Implant Direct Sybron Manufacturing, LLC62023

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

Recent FDA clearances

Adin Long Dental Implant System · Adin Dental Implant Systems , Ltd.510(k) · 2026-03-23
ZENEX Implant System_Short (R-System) · Izenimplant Co., Ltd.510(k) · 2026-03-16
Straumann® BLC Implants - Indication Widening · Institut Straumann AG510(k) · 2026-03-10
Dentis SQ-SL AXEL Fixture · Dentis Co., Ltd.510(k) · 2026-03-04
Nobel Biocare S Series Implants · Nobel Biocare AB510(k) · 2026-02-18
BIORES Dental Implant System · Chengdu Besmile Medical Technology Co., Ltd.510(k) · 2026-02-02
ZENEX Implant System_R-System · Izenimplant Co., Ltd.510(k) · 2026-01-08
GEN5™ and GEN5+™ 3.3mmD Dental Implants · Paragon Implant Mfg., LLC510(k) · 2025-12-23
NizPlant Dental Implant System · Paragon Implant Mfg., LLC510(k) · 2025-12-23
DIMPLO Implant System · DIMPLO, Ltd.510(k) · 2025-12-22
Pterygoid Indication for GM Helix Implants · JJGC Indústria e Comércio de Materiais Dentários S.A.510(k) · 2025-12-12
S.I.N. Tapered Pro Conical Zygoma Implant System · S.I.N. Implant System Ltda510(k) · 2025-11-07
GEN5 and GEN5+ Dental Implant System · Paragon Implant Mfg., LLC510(k) · 2025-10-30
HexaPLUS S OneDrill Implant System · Osseofuse International, Inc.510(k) · 2025-10-10
Paltop Dental Implant System · Paltop Advanced Dental Solutions, Ltd.510(k) · 2025-09-29
S.I.N. Dental Implant System · S.I.N. Implant System Ltda510(k) · 2025-09-26
JDEvolution Plus L and JDEvolution Plus LE · Jdentalcare Srl510(k) · 2025-09-25
NobelZygoma TiUltra Implant system · Nobel Biocare AB510(k) · 2025-08-25
MIS C1 Implant System, MIS Seven Implant System, MIS M4 Implant System, MIS Lance+ Implant System, MIS Lance+ Conical Connection System · Dentsply Sirona, Inc.510(k) · 2025-08-21
Neodent Implant System - Zirconia Implant System · JJGC Indústria e Comércio de Materiais Dentários S.A.510(k) · 2025-08-18
S.I.N. Dental Implant System · S.I.N. Implant System Ltda510(k) · 2025-08-13
Straumann® RidgeFit Implants · Institut Straumann AG510(k) · 2025-08-12
MIS LYNX Conical Connection Implant System · Dentsply Sirona, Inc.510(k) · 2025-07-24
DESS® Dental Implants · Terrats Medical SL510(k) · 2025-07-23
SD TL Implant System · Arum Dentistry Co., Ltd.510(k) · 2025-07-23

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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