13 results
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21ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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Omni-Directional Multi-unit Abutment System (Trade Name: Omnibut)
FDA 510(k)
FDA Class 2
·Dental
VERTE-STACK® Spinal System
FDA UDI
MEDTRONIC SOFAMOR DANEK, INC.·00613994304902·STRUT 6242064 ANATOMIC 16X14X24MM
VERTE-STACK® Spinal System
FDA UDI
MEDTRONIC SOFAMOR DANEK, INC.·00763000856700·STRUT 6242064 ANATOMIC 16X14X24MM
NA
FDA UDI
Medos International Sàrl·10886705031702·Button Trocar Compatible with 3.5 mm Endoscopic...
Admiral ACP System
FDA 510(k)
FDA Class 2
·Orthopedic
GALILEO NT
FDA 510(k)
FDA Class 2
·Neurology
IMP,TSV,4.1MM,SBM,16
FDA Adverse Event
Injury
·ZIMMER DENTAL·Product code DZE·September 20, 2023
IMP,TSV,4.1MM,SBM,16
FDA Adverse Event
Injury
·ZIMMER DENTAL·Product code DZE·September 20, 2023
NA
FDA UDI
Zimmer, Inc.·00889024119628·
ALARIS SYSTEM
FDA Adverse Event
Malfunction
·CAREFUSION SD·Product code FRN·November 2, 2023
UNKNOWN MESH PRODUCT (EWHU)
FDA Adverse Event
Injury
·ETHICON INC·Product code FTL·September 9, 2011
ONETOUCHPING GLUCOSEMGMTSYSTEM
FDA Adverse Event
Malfunction
·ANIMAS CORPORATION·Product code LZG·November 10, 2014
OT VERIO IQ METER
FDA Adverse Event
Malfunction
·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·July 23, 2013