17 results
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20ms
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Sources: EU EUDAMED, US FDA
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Regulation: Us FDA
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Xperius Ultrasound System
FDA 510(k)
FDA Class 2
·Radiology
BIO PLUG
FDA UDI
Biomet Orthopedics, LLC·00880304004108·
MEGA SPINE SYSTEM
FDA UDI
BK MEDITECH CO.,LTD.·08809763500756·Multi Screw Driver
MSI Precision Specialty Instruments
FDA UDI
Med Saver, Inc.·00194613123000·Instrument Guards, Tinted, Assorted Package, Ve...
Needle Holder
FDA UDI
KATENA PRODUCTS, INC.·00841668108246·BARRAQUER NEEDLE HOLDER CURVED WITH LOCK
Cosmolock
FDA UDI
Kalitec Direct LLC·B07311K1430200·Rod Template, 250mm
Endo-Model SL Knee Prosthesis System
FDA UDI
WALDEMAR LINK GmbH & Co. KG·04026575417162·Proximal Tibial Spacer,
Endo-Model SL Knee Prosthesis System
FDA UDI
WALDEMAR LINK GmbH & Co. KG·04026575417131·Proximal Tibial Spacer,
MSI Precision Specialty Instruments
FDA UDI
Med Saver, Inc.·00194613044633·Assorted Vented Tinted Micro Guards, (100 Total...
Endo-Model SL Knee Prosthesis System
FDA UDI
WALDEMAR LINK GmbH & Co. KG·04026575417193·Proximal Tibial Spacer,
INTAI BONE PLATE AND BONE SCREW SYSTEM; INTAI DHS/DCS PLATE SYSTEM
FDA 510(k)
FDA Class 2
·Orthopedic
ATLANTIS ABUTMENT FOR KEYSTONE IMPLANT, ATLANTIS GEMINI ABUTMENT
FDA 510(k)
FDA Class 2
·Dental
KANGAROO
FDA Adverse Event
Malfunction
·CARDINAL HEALTH 200, LLC·Product code KNT·October 16, 2024
TENSION FREE VAGINAL TAPE
FDA Adverse Event
Injury
·ETHICON, INC.·Product code FTL·June 11, 2013
UNICEL® DXC 800 PRO SYNCHRON® CHEMISTRY ANALYZER
FDA Adverse Event
Malfunction
·BECKMAN COULTER INC.·Product code JJE·July 15, 2011
CAPSURE SP
FDA Adverse Event
Malfunction
·MPRI·Product code DTB·October 10, 2014
XP-XP Tibial Tray - Interlok 73 mm Item # 195756
FDA Enforcement
Class II
·Terminated·Zimmer Biomet, Inc.·September 18, 2019