DYBFDA Class 2 · 21 CFR 870.1340

Introducer, Catheter

Device family · Cardiovascular

Automated profile from regulatory + adverse-event registries · AI-reviewed · expert clinical sign-off in progress — not yet independently verified.
FDA clearances
700
Manufacturers
106
Flagged signals
23
Adverse-event reports
32,967

Code matrix

FDA product codeDYB
Device classClass 2
Regulation21 CFR 870.1340
GMDN— (crosswalk pending)
ImplantableNo
Life-sustainingNo

Adverse-event signals

Public · always free

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

Event typeYearReportsPRRχ²
Other2010445.1131
Death2025425.271
Other2010919.0136
Death2025615.166
Other2010413.334
Death2015513.245
Death2026129.785
Other200936.39
Death201485.727
Death201535.47
Death20241063.3165
Death202553.05
Death2025892.797
Death2023892.797
Death2023272.728
Death2025102.47
Death2022752.355
Death2021222.214
Death2022222.214
Death2024222.214
Injury20221732.1154
Injury202372.04
Death2025152.07

Device-level recall linkage pending an FDA-recalls product-code re-ingest. Class 2 family · 32,967 total adverse-event reports.

Manufacturer landscape

ManufacturerClearancesLatestConcern
St Jude Medical212014
Terumo Medical Corp.192011
Cordis Corp.192000
Daig Corp.182000
Merit Medical Systems, Inc.182025
COOK INCORPORATED1720210.23
C.R. Bard, Inc.162021
Oscor, Inc.132021
Arrow Intl., Inc.92002
B.Braun Medical, Inc.92004
Edwards Lifesciences, LLC82014
TERUMO MEDICAL CORPORATION82020
Boston Scientific Corp82015
W. L. Gore & Associates, Inc.72016
Great Batch Medical72018
Abiomed, Inc.62025
Norton Performance Plastics Corp.61983
Medtronic Vascular62016
ACUTUS MEDICAL, INC.62023
BOSTON SCIENTIFIC CORPORATION620230.14
ARGON MEDICAL DEVICES, INC.62025
Quinton, Inc.51987
Datascope Corp.52000
ACCESS SCIENTIFIC, LLC52019
ST. JUDE MEDICAL, INC.52016

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

Recent FDA clearances

Introducer Sheath Set · Cardiocycle Medical(Suzhou) Co., Ltd.510(k) · 2026-04-23
Edwards eSheath+ introducer set · Edwards Lifesciences510(k) · 2026-04-17
Aventus Introducer Sheath · Inquis Medical510(k) · 2026-04-13
Protaryx Transseptal Puncture Device (PTX2-001) · Protaryx Medical, Inc.510(k) · 2026-04-10
AuST Steerable Sheath · CenterPoint Systems, LLC510(k) · 2026-04-07
VANES Delivery System (VDS) · Zoll Respicardia, Inc.510(k) · 2026-04-06
Multiflex Steerable Sheath 17.5F · Vizaramed, Inc.510(k) · 2026-03-26
AuST CSP Introducer · CenterPoint Systems, LLC510(k) · 2026-02-19
Peel-Away Introducer Sheath · VascuTech Medical, LLC510(k) · 2026-02-09
Genie MAX Large Bore Introducer Sheath · Cultiv8 1, LLC510(k) · 2026-01-22
Intri26 Introducer Sheath · Inari Medical, Inc.510(k) · 2025-12-17
V•Stick™ Vascular Access Set · Argon Medical Devices, Inc.510(k) · 2025-12-15
PerQseal Introducers · Vivasure Medical Limited510(k) · 2025-10-23
Introducer Sheath Set · Cardiocycle Medical(Suzhou) Co., Ltd.510(k) · 2025-10-21
14Fr Low Profile Introducer Kit · Abiomed, Inc.510(k) · 2025-10-08
Primero Safe Access System · South53, LLC510(k) · 2025-09-29
Pounce(TM) Sheath · Surmodics,Inc.510(k) · 2025-09-24
Vertex(TM) Catheter · Jupiter Endovascular510(k) · 2025-09-12
Edwards eSheath Optima introducer set · Edwards Lifesciences510(k) · 2025-08-29
AuST Steerable Sheath · CenterPoint Systems, LLC510(k) · 2025-04-30
Prelude Wave Hydrophilic Sheath Introducer · Merit Medical Systems, Inc.510(k) · 2025-04-25
PeriCross™ Epicardial Access Kit · Circa Scientific, Inc.510(k) · 2025-04-24
Edwards eSheath Optima introducer set · Edwards Lifesciences510(k) · 2025-03-27
iSLEEVE Introducer Set · Boston Scientific510(k) · 2025-03-20
ViaOne Epicardial Access System · Cardiovia , Ltd.510(k) · 2025-03-20

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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