10 results
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19ms
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Sources: EU EUDAMED, US FDA
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Regulation: Us FDA
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SYNTHES 1.5MM/2.0MM ORTHOGNATHIC MAXILLARY PLATES AND SCREWS
FDA 510(k)
FDA Class 2
·Dental
1.85MM TI MATRIX SCREW SELF-TAPPING/4MM
FDA Adverse Event
Malfunction
·SYNTHES (USA)·Product code JEY·January 21, 2015
DeltaForm HD
FDA UDI
Merz Dental GmbH·D7091980199·DeltaForm HD lower posteriors, XS, BL4 -MADE IN...
All Purpose Cuff
FDA UDI
SUNTECH MEDICAL, INC.·10840935109167·
SYMMETRIC TOTAL KNEE SYSTEM
FDA 510(k)
FDA Class 2
·Orthopedic
BIO-C TEMP
FDA 510(k)
FDA Class 2
·Dental
CODEMASTER XL
FDA Adverse Event
Malfunction
·AGILENTTECHNOLOGIES, INC.·Product code LDD·February 2, 2013
EXTRACTION SCREW FOR PFNA BLADE
FDA Adverse Event
Malfunction
·SYNTHES BETTLACH·Product code HWB·August 5, 2014
VERSYS HIP SYSTEM FEMORAL HEAD
FDA Adverse Event
Injury
·ZIMMER·Product code LPH·February 1, 2011
Angiotech Pediatric Bone Marrow Needle. Pediatric Bone Marrow Needle. STERILE. Product Number: ION18015. 510k K980196. MEDICAL DEVICE TECHNOLOGIES, INC. 3600 Southwest 74th Avenue, Gainesville, Florida 32608 U.S.A. Intended Use: Pediatric Bone Marrow Needle
FDA Recall
Terminated
·Medical Device Technologies, Inc.·Product code KNW·September 1, 2009