19 results
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21ms
·
Sources: EU EUDAMED, US FDA
EXPANDABLE PEEK VBR IMPLANT
FDA 510(k)
FDA Class 2
·Orthopedic
TASMIN R 4°
FDA UDI
SIGNUS Medizintechnik GmbH·04047844014479·The basic shape of the TASMIN R devices is a ho...
CoRoent
FDA UDI
Nuvasive, Inc.·00887517282736·CoRoent® Large MP, 9x9x28 4°
FIX-L PEEK PLIF and T-PLIF System
FDA UDI
Jeil Medical Corporation·08800089469741·
FIX-L PEEK PLIF and T-PLIF System
FDA UDI
Jeil Medical Corporation·08800089469727·
FIX-L PEEK PLIF and T-PLIF System
FDA UDI
Jeil Medical Corporation·08800089469819·
FIX-L PEEK PLIF and T-PLIF System
FDA UDI
Jeil Medical Corporation·08800089469789·
FIX-L PEEK PLIF and T-PLIF System
FDA UDI
Jeil Medical Corporation·08800089469796·
FIX-L PEEK PLIF and T-PLIF System
FDA UDI
Jeil Medical Corporation·08800089469765·
FIX-L PEEK PLIF and T-PLIF System
FDA UDI
Jeil Medical Corporation·08800089469772·
FIX-L PEEK PLIF and T-PLIF System
FDA UDI
Jeil Medical Corporation·08800089469734·
FIX-L PEEK PLIF and T-PLIF System
FDA UDI
Jeil Medical Corporation·08800089469758·
FIX-L PEEK PLIF and T-PLIF System
FDA UDI
Jeil Medical Corporation·08800089469802·
PROLITE VL PULSED LIGHT SYSTEM
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
QUINUPRISTIN/DALFOPRISTIN ANTIMICROBIAL SUSCEPTIBILITY TEST DISC
FDA 510(k)
FDA Class 2
·Microbiology
COATED VICRYL PLUS ANTIBACTERIAL (POLYGLACTIN 910)
FDA Adverse Event
Malfunction
·ETHICON, INC.·Product code GAM·April 8, 2013
RESTORE ULTRA
FDA Adverse Event
Malfunction
·MDT PUERTO RICO OPERATIONS CO., JUNCOS·Product code LGW·March 23, 2011
LIFELINE AED
FDA Adverse Event
Malfunction
·DEFIBTECH, LLC·Product code MKJ·May 9, 2008
The Spirit Select Bed, Model 5700 Spirit Plus /with high rail siderail option
FDA Enforcement
Class II
·Terminated·Stryker Medical Division of Stryker Corporation·November 21, 2018