16 results
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22ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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IMAGE WORKS PANOURA
FDA 510(k)
FDA Class 2
·Dental
MEDI
FDA UDI
MEDI MANUFACTURING, INC.·04049772814572·GENUMEDI SAND SIZE VI
ArgenZ HT+ 95x25 OM1
FDA UDI
ARGEN CORPORATION, THE·D818122806·Dental porcelain/ceramic restoration kit
Millennium
FDA UDI
Avalign Technologies, Inc.·00190776305352·House Inferior Turbinate Submuccous Resection S...
NATRELLE 133 TISSUE EXPANDER WITH SUTURE TABS
FDA 510(k)
FDA Unclassified
·Unknown
DUOPRO SAFETY SYRINGE (DUOPROSS)
FDA 510(k)
FDA Class 2
·General Hospital
BD VEO¿ INSULIN SYRINGES WITH BD ULTRA-FINE¿ NEEDLE
FDA Adverse Event
Malfunction
·BD MEDICAL - DIABETES CARE·Product code FMF·June 14, 2023
TARGET DEVICE 300X160MM
FDA Adverse Event
Malfunction
·STRYKER OSTEOSYNTHESIS KIEL·Product code LXH·March 2, 2012
GMK STANDARD CEMENTED FEMUR SIZE 5 LEFT
FDA Adverse Event
Injury
·MEDACTA INTERNATIONAL, SA·Product code JWH·December 19, 2013
ARCTIC FRONT ADVANCE CARDIAC CRYOABLATION CATHETER
FDA Adverse Event
Injury
·MEDTRONIC, INC.·Product code OAE·December 15, 2020
ARCTIC FRONT ADVANCE CARDIAC CRYOABLATION CATHETER
FDA Adverse Event
Injury
·MEDTRONIC, INC.·Product code OAE·December 15, 2020
ONETOUCHPING GLUCOSEMGMTSYSTEM
FDA Adverse Event
Malfunction
·ANIMAS CORPORATION·Product code LZG·May 21, 2013
MINICAP TRANSFER SET
FDA Adverse Event
Injury
·BAXTER HEALTHCARE - MOUNTAIN HOME·Product code KDJ·June 14, 2011
COAGUCHEK S SYSTEM
FDA Adverse Event
Malfunction
·ROCHE DIAGNOTICS·Product code JPA·August 14, 2008
OPTETRAK
FDA Adverse Event
Injury
·EXACTECH, INC.·Product code JWH·September 2, 2022
4.5 mm TRIVEX System Resector Kit (blade and tubing), 3 per box Part Number: 7209514
FDA Recall
Terminated
·Smith & Nephew, Inc. Endoscopy Division·Product code GEI·June 19, 2006