10 results
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22ms
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Sources: EU EUDAMED, US FDA
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Regulation: Us FDA
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Laparoscopic Curved Spatula Electrode, Retractable, Aspiration Hole, 28cm ; Laparoscopic Wire J-Hook Electrode, Retractable, Aspiration Hole, 28cm ; Laparoscopic Wire L-Hook Electrode, Retractable, Aspiration Hole, 28cm; Laparoscopic Wire L-Hook Electrode, Retractable, Aspiration, 36cm ; Laparoscopic Flat L-Hook Electrode, Retractable, Aspiration Hole, 28cm ; Laparoscopic Straight Spatula Electrode, Hollow, 28cm ; Laparoscopic Curved Spatula Electrode, Hollow, 28cm; Laparoscopic Wire J
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
Vanguard® Knee System
FDA UDI
Biomet Orthopedics, LLC·00880304271760·
Millennium
FDA UDI
Avalign Technologies, Inc.·00190776403027·MALLEABLE SLOTTED BLADE 6" X 6"
Collis Curve Toothbrush
FDA registration
Collis Curve Toothbrush·1 product·🇺🇸 United States
TOTAL KNEE REPLACEMENT CEMENT KLASSIC TOTAL KNEE SYSTEM
FDA Adverse Event
Injury
·TOTAL JOINT ORTHOPEDICS, INC.·Product code JWH·August 18, 2020
EZ HSG CATHETER.FOAMSEAL CATHETER
FDA 510(k)
FDA Class 2
·Obstetrics/Gynecology
PONTO PRO POWER
FDA 510(k)
FDA Class 2
·Ear, Nose, Throat
COLLEAGUE CX VOLUMETRIC INFUSION PUMP
FDA Adverse Event
Malfunction
·BAXTER HEALTHCARE PTE. LTD.·Product code FRN·October 4, 2008
UNICEL DXC 800 SYNCHRON SYSTEM
FDA Adverse Event
Malfunction
·BECKMAN COULTER, INC.·Product code JGS·July 8, 2011
ADAPT F/BLADE F/REMOVAL OF PFNA-BLADES
FDA Adverse Event
Malfunction
·SYNTHES GMBH·Product code HWE·June 22, 2013