48 results
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21ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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DEPUY CANNULATED BONE SCREW
FDA 510(k)
FDA Class 2
·Orthopedic
Medtronic Reusable Instruments
FDA UDI
MEDTRONIC SOFAMOR DANEK, INC.·00673978164922·DISTRACTOR SHAFT EXTENSION
APEX Knee System
FDA UDI
Omni Life Science, Inc.·00841690198314·AK3 PS Insert Trial Size 5, 12mm
Arthrex®
FDA UDI
ARTHREX, INC.·00888867131934·LO-PRO SCRW,TI,3.5MMX 12MM
THD Procto Software System
FDA 510(k)
FDA Class 2
·Radiology
ENCOR BREAST BIOPSY SYSTEM
FDA 510(k)
FDA Class 2
·Gastroenterology, Urology
LOCKING SCREW, TITANIUM 3.5MM X 14MM
FDA Adverse Event
Injury
·ARTHREX, INC.·Product code HRS·September 19, 2018
LO-PRO LOCK SCRW,TI,3.5MMX 12MM
FDA Adverse Event
Injury
·ARTHREX, INC.·Product code HRS·September 19, 2018
2.4 X 20MM VAL SCREW, TI
FDA Adverse Event
Injury
·ARTHREX, INC.·Product code HRS·September 19, 2018
LO-PRO SCRW,TI,3.5MMX 12MM
FDA Adverse Event
Injury
·ARTHREX, INC.·Product code HRS·September 19, 2018
VOLAR DISTAL RAD PLT TI NARROW LT 3H
FDA Adverse Event
Injury
·ARTHREX, INC.·Product code HRS·September 19, 2018
G4 PLATINUM CONTINUOUS GLUCOSE MONITORING SYSTEM
FDA Adverse Event
Malfunction
·DEXCOM, INC.·Product code MDS·July 6, 2015
ADVANCE
FDA Adverse Event
Malfunction
·HILL-ROM, INC.·Product code FNL·February 14, 2014
OT ULTRAMINI
FDA Adverse Event
Injury
·LIFESCAN INC.·Product code NBW·November 8, 2010
WRIST SPANNING PLATE, TI
FDA Adverse Event
Injury
·ARTHREX, INC.·Product code HRS·December 26, 2019
LOW PROFILE SCREW, 2.4 X 10MM, CORTEX
FDA Adverse Event
Injury
·ARTHREX, INC.·Product code HWC·January 9, 2020
2.4 X 10MM VAL SCREW, TI
FDA Adverse Event
Injury
·ARTHREX, INC.·Product code HRS·January 9, 2020
LO-PRO LOCK SCRW,TI,3.5MMX 12MM
FDA Adverse Event
Injury
·ARTHREX, INC.·Product code HRS·January 9, 2020
LO-PRO LOCK SCRW,TI,3.5MMX 12MM
FDA Adverse Event
Injury
·ARTHREX, INC.·Product code HRS·January 9, 2020
2.4 X 16MM VAL SCREW, TI
FDA Adverse Event
Injury
·ARTHREX, INC.·Product code HRS·January 9, 2020