156 results · 30ms · Sources: EU EUDAMED, US FDA

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Intraocular Lens

FDA Pre-Market Approval
FDA Class 3 ·MODELS A21-A & A21-B POSTERIOR CHAMBER INTRAOCULAR

ACE

FDA UDI
ACE SURGICAL SUPPLY CO., INC.·00614950022939·SUCTION TIP ENDODONTIC TYPE TIP OPENING 1MM 6" ...

Master Series

FDA UDI
AMERICAN ORTHODONTICS CORPORATION·00190746095207·DB BRACKET MASTER SERIES MAX LEFT BICUSPID 022 ...

Master Series

FDA UDI
AMERICAN ORTHODONTICS CORPORATION·00190746096501·DB BKT MASTER IBD UR LAT 022 T+14 A+9 R=0

KESTREL LENS CASE 731H-893S/P-1700-2611

FDA 510(k)
FDA Class 2 ·Ophthalmic

AMS 700 LGX

FDA Adverse Event
Injury ·BOSTON SCIENTIFIC CORPORATION·Product code JCW·September 23, 2025

AMS 700 LGX

FDA Adverse Event
Injury ·BOSTON SCIENTIFIC CORPORATION·Product code JCW·September 2, 2025

ROTAPRO

FDA Adverse Event
Malfunction ·BOSTON SCIENTIFIC CORPORATION·Product code MCX·October 15, 2025

ROTABLATOR?

FDA Adverse Event
Malfunction ·BOSTON SCIENTIFIC CORPORATION·Product code MCW·May 5, 2025

ROTABLATOR?

FDA Adverse Event
Malfunction ·BOSTON SCIENTIFIC CORPORATION·Product code MCW·April 4, 2025

CENTURION VISION SYSTEM

FDA Adverse Event
Injury ·ALCON - IRVINE TECHNOLOGY CENTER·Product code HQC·May 27, 2014

RSVR MMT-326A 10PK PRDGM 1.8ML 13L

FDA Adverse Event
Malfunction ·MEDTRONIC MINIMED·Product code FMF·November 8, 2010

AED PLUS

FDA Adverse Event
Malfunction ·ZOLL MEDICAL CORPORATION·Product code MKJ·December 26, 2012

Device, Incontinence, Mechanical/Hydraulic

FDA Pre-Market Approval
FDA Class 3 ·AMS SPHINCTER 800 URINARY CONTROL SYSTEM

Kit, Assay, Progesterone Receptor

FDA Pre-Market Approval
FDA Class 3 ·ABBOTT PGR-EIA MONOCLONAL

STEALTHSTATION¿ S8 SYSTEM

FDA Adverse Event
Malfunction ·MEDTRONIC NAVIGATION, INC·Product code HAW·April 4, 2024

AMS 700 LGX

FDA Adverse Event
Injury ·BOSTON SCIENTIFIC CORPORATION·Product code JCW·January 19, 2026

Device, Incontinence, Mechanical/Hydraulic

FDA Pre-Market Approval
FDA Class 3 ·AMS 800 URINARY CONTROL SYSTEM

Device, Incontinence, Mechanical/Hydraulic

FDA Pre-Market Approval
FDA Class 3 ·AMS 800 URINARY CONTROL SYSTEM

Device, Incontinence, Mechanical/Hydraulic

FDA Pre-Market Approval
FDA Class 3 ·AMS 800™ Artificial Urinary Sphincter (AUS)