27 results
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22ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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MODIFIED FREEMAN ACETABULAR CUP
FDA 510(k)
FDA Class 3
·Orthopedic
Affymterix
FDA UDI
Affymetrix, Inc.·00856826006135·CytoScan™ Dx Post-PCR 2-8°C MOD S AH W PB
Corneal Trephine
FDA UDI
KATENA PRODUCTS, INC.·00841668112793·BARRON VACUUM PUNCH 8.5MM
OsteoVation
FDA UDI
SKELETAL KINETICS LLC·00813845020092·OsteoVation Impact Bone Void Filler
Mariner
FDA UDI
Seaspine Orthopedics Corporation·10889981142179·Mariner Implant Tray, Screw Caddy
BOSS Instruments
FDA UDI
BOSS INSTRUMENTS, LTD., INC.·00888515227378·Schuknecht Wire Crimper, 6mm jaws
Elite®
FDA UDI
Ortho Organizers, Inc.·00190707051679·.022/045 U6L CBT/NC -10T 5 OFF
SPL CRIMP SYSTEM
FDA 510(k)
FDA Class 2
·Orthopedic
WAVEON FRACTURE REPAIR SYSTEM (WAVEON RX)
FDA 510(k)
FDA Class 2
·Orthopedic
Truliant
FDA UDI
Exactech, Inc.·10885862522634·TRULIANT 10MM SHIM FOR SPACER BLOCK
PREMIER ANTERIOR CERVICAL PLATE SYSTEM
FDA Adverse Event
Injury
·WARSAW ORTHOPEDIC, INC.·Product code KWQ·August 12, 2011
PREMIER® ANTERIOR CERVICAL PLATE SYSTEM
FDA Adverse Event
Injury
·WARSAW ORTHOPEDICS·Product code KWP·March 3, 2017
PREMIER® ANTERIOR CERVICAL PLATE SYSTEM
FDA Adverse Event
Injury
·MDT SOFAMOR DANEK PUERTO RICO MFG·Product code KWP·March 3, 2017
PREMIER® ANTERIOR CERVICAL PLATE SYSTEM
FDA Adverse Event
Malfunction
·MEDTRONIC SOFAMOR DANEK·Product code KWP·May 7, 2015
SYMBIQ SCHANNEL 3.01
FDA Adverse Event
Malfunction
·HOSPIRA COSTA RICA LTD.·Product code FRN·May 2, 2014
ONETOUCHPING GLUCOSEMGMTSYSTEM
FDA Adverse Event
Malfunction
·ANIMAS CORPORATION·Product code LZG·January 8, 2013
COBAS 6000 C501 MODULE
FDA Adverse Event
Malfunction
·ROCHE DIAGNOSTICS·Product code CEM·November 18, 2010
VANGUARD ILOK FEMORAL COMPONENT
FDA Adverse Event
Injury
·ZIMMER BIOMET, INC.·Product code JWH·May 2, 2018
BIOMET CRUCIATE TIBIAL TRAY
FDA Adverse Event
Injury
·ZIMMER BIOMET, INC.·Product code JWH·May 2, 2018
VANGUARD TIBIAL BEARING
FDA Adverse Event
Injury
·ZIMMER BIOMET, INC.·Product code JWH·May 2, 2018