41 results
·
22ms
·
Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
×
Self-retaining Retractor
FDA 510(k)
FDA Class 2
·Neurology
Cohere
FDA UDI
Nuvasive, Inc.·00195377028136·COHERE TLIF-O Trial, 16x10mm 4°
OsteoMed
FDA UDI
OSTEOMED LLC·00845694033985·Logic Jr. 52mm Right Short Distractor,15mm Dist...
Sentry Dental TC&B
FDA UDI
NU RADIANCE INC·00815143001933·Sentry Dental TC&B Shade A3
Vilex Power Accessory
FDA UDI
VILEX IN TENNESSEE, INC.·00841731122254·KWire .062x4" (1.6x100mm)
UniTip Catheter
FDA UDI
Unisensor AG·07640172973226·
HANSEN MEDICAL VASCULAR CATHETER CONTROL SYSTEM AND CATHETER
FDA 510(k)
FDA Class 2
·Cardiovascular
ATLANTIS ABUTMENT FOR DENTSPLY ANKYLOS IMPLANT, ATLANTIS GEMINI ABUTMENT, ATLANTIS GEMINI + ABUTMENT
FDA 510(k)
FDA Class 2
·Dental
CARELINK
FDA Adverse Event
Malfunction
·MEDTRONIC, INC.·Product code KRG·October 10, 2014
OT VERIO IQ METER
FDA Adverse Event
Malfunction
·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·June 11, 2013
UNICEL DXI 800 ACCESS IMMUNOASSAY SYSTEM
FDA Adverse Event
Malfunction
·BECKMAN COULTER, INC.·Product code JJE·June 17, 2011
SHIRANUI EX
FDA Adverse Event
Injury
·KANEKA CORPORATION·Product code LIT·September 11, 2022
SHIRANUI EX
FDA Adverse Event
Injury
·KANEKA CORPORATION·Product code LIT·April 14, 2026
SHIRANUI EX
FDA Adverse Event
Injury
·KANEKA CORPORATION·Product code LIT·May 24, 2021
SHIRANUI EX
FDA Adverse Event
Injury
·KANEKA CORPORATION·Product code LIT·January 11, 2022
SHIRANUI EX
FDA Adverse Event
Injury
·KANEKA CORPORATION·Product code LIT·January 29, 2026
SHIRANUI HP
FDA Adverse Event
Injury
·KANEKA CORPORATION·Product code LIT·May 18, 2020
SHIRANUI EX
FDA Adverse Event
Injury
·KANEKA CORPORATION·Product code LIT·October 22, 2024
SHIRANUI EX
FDA Adverse Event
Injury
·KANEKA CORPORATION·Product code LIT·August 12, 2020
SHIRANUI HP
FDA Adverse Event
Malfunction
·KANEKA CORPORATION·Product code LIT·April 24, 2019