36 results
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21ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: 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