36 results · 21ms · Sources: EU EUDAMED, US FDA

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COLLEXA

FDA 510(k)
FDA Unclassified ·Unknown

MT

FDA UDI
Micro-Tech (Nanjing) Co., Ltd.·06932503540346·Normal handle, Oval, without spike, Single out...

SATINSKY NEONATAL CLAMP

FDA UDI
SONTEC INSTRUMENTS, INC.·B09921005740·SATINSKY NEONATAL CLAMP

MINI NEUROLOGICAL RONGEUR

FDA UDI
SONTEC INSTRUMENTS, INC.·00192896048096·MINI NEUROLOGICAL RONGEUR STRAIGHT TIP

House Brand Dentistry

FDA UDI
Frontier Dental Supply Inc·00810189432451·HSB - CSR Wrap 24 x 24 - 100/Sheets

Merit Medical®

FDA UDI
Merit Medical Systems, Inc.·00884450456767·

HS Diam. Burr, Ø2.3x95, 80k

FDA UDI
Bien-Air Surgery SA·17630055507157·

Merit Medical®

FDA UDI
Merit Medical Systems, Inc.·00884450267356·

N/A

FDA UDI
Doppkon GmbH & Co. KG·04262494462528·Guide Wire Ø 0,8mm, WL 450mm

POWDER FREE VINYL PATIENT EXAMINATION GLOVES, COLORED (YELLOW)

FDA 510(k)
FDA Class 1 ·General Hospital

IONTOPHORETIC DRUG DELIVERY ELECTRODE, IONTOPHORETIC ELECTRODE (ACTIVE)

FDA 510(k)
FDA Class 2 ·Physical Medicine

Q-SYTE

FDA Adverse Event
Malfunction ·BECTON DICKINSON INFUSION THERAPY SYSTEMS INC.·Product code FPA·February 4, 2026

EVERCROSS

FDA Adverse Event
Injury ·PLYMOUTH-PA·Product code DQY·September 24, 2015

ONE TOUCH LANCING DEVICE

FDA Adverse Event
Injury ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·September 19, 2014

TERUMO PERFUSION SYSTEM 8000

FDA Adverse Event
Malfunction ·TERUMO CARDIOVASCULAR SYSTEMS CORP.·Product code JOR·May 13, 2011

Custom Waste Management Kit: REF: K10-00353K, K10-01603C, K10-01694Q, K10-05159B, K10-05743, K10-05825AP

FDA Enforcement
Class II ·Ongoing·Merit Medical Systems, Inc.·August 20, 2025

Custom Waste Management Kit: REF: K10-00353K, K10-01603C, K10-01694Q, K10-05159B, K10-05743, K10-05825AP

FDA Recall
Open, Classified ·Merit Medical Systems, Inc.·Product code PPD·June 5, 2025

SPECTRUM TURBO-JECT ANTIBIOTIC POWER INJECTABLE PICC

FDA Adverse Event
Injury ·COOK INC·Product code FOZ·April 2, 2019

SPECTRUM TURBO-JECT ANTIBIOTIC POWER INJECTABLE PICC

FDA Adverse Event
Malfunction ·COOK INC·Product code FOZ·March 14, 2018

LJS TURBO-JECT PERIPHERALLY INSERTED CENTRAL VENOUS CATHETER

FDA Adverse Event
Injury ·COOK INC·Product code LJS·May 11, 2018