11 results
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19ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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CHEMTRUE SINGLE/MULTI-PANEL DRUG SCREEN DIP CARD/ CASSETTE TESTS
FDA 510(k)
FDA Class 2
·Clinical Toxicology
Protective Cap
FDA UDI
BIO CONCEPT Co., Ltd.·06947600381488·
Forestanit®
FDA UDI
Forestadent Bernhard Förster GmbH·EFOR21230801·Forestanit wire round hard clinic coil 0,80 mm
CosmoLock Pedicle Screw System
FDA UDI
Kalitec Direct LLC·B07311K1230000·Rod Holder, Curved, 5.5 mm
GALIX PACESTAR
FDA 510(k)
FDA Class 2
·Cardiovascular
ALBOGRAFT VASCULAR PROSTHESIS
FDA 510(k)
FDA Class 2
·Cardiovascular
NA
FDA Adverse Event
Injury
·BOSTON SCIENTIFIC NEUROMODULATION·Product code MHY·September 12, 2019
NON AC-POWERED PATIENT LIFT
FDA Adverse Event
HENYI ENTERPRISE·Product code FSA·May 21, 2013
ONETOUCHPING GLUCOSEMGMTSYSTEM
FDA Adverse Event
Malfunction
·ANIMAS CORPORATION·Product code LZG·September 26, 2014
FLEXCATH STEERABLE SHEATH
FDA Adverse Event
Malfunction
·MEDTRONIC CRYOCATH LP·Product code DRA·June 14, 2011
BIOMET StageOne Knee Femoral Cement Spacer Mold, 65 MM, Silicone, Sterile, Item 432165.
FDA Enforcement
Class II
·Terminated·Biomet, Inc.·April 15, 2020