23 results · 31ms · Sources: EU EUDAMED, US FDA

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SECULOK™ ACP System

FDA 510(k)
FDA Class 2 ·Orthopedic

Oticon

FDA UDI
Oticon A/S·05707131340870·G500 FW 6.0

Pre-Finisher

FDA UDI
TP ORTHODONTICS INC·00192029041550·Non-Extraction

N/A

FDA UDI
DENTSPLY SIRONA ORTHODONTICS INC.·D807K190055001·MTM® NO TRACE (TM) 018 UL/4-4

IN-OVATION® L

FDA UDI
DENTSPLY SIRONA ORTHODONTICS INC.·D807K190055011·IN-OVATION® L 018 UPPER 6-6

Cosmolock

FDA UDI
Kalitec Direct LLC·B07311K1100530·Caddie, 7.5mm Screws

IN-OVATION® L

FDA UDI
DENTSPLY SIRONA ORTHODONTICS INC.·D807K190055101·IN-OVATION® L 018 UL/7-7

MATTIOLI PULSE TWO/THREE PLUS FAMILY

FDA 510(k)
FDA Class 2 ·General, Plastic Surgery

APTUS 2.0 RADIAL HEAD SYSTEM

FDA 510(k)
FDA Class 2 ·Orthopedic

BD PEN NDL 31GA 8MM

FDA Adverse Event
Malfunction ·BECTON DICKINSON AND CO.·Product code FMI·September 17, 2021

SOF-FLEX MULTI-LENGTH URETERAL STENT SET

FDA Adverse Event
Malfunction ·COOK INC·Product code FAD·October 24, 2024

G7 NEUTRAL E1 LINER 36MM D

FDA Adverse Event
Malfunction ·ZIMMER BIOMET, INC.·Product code PBI·February 28, 2018

2.4MM TI LOCKING SCREW 12MM F/LOCKING RECONSTRUCTION PLATE

FDA Adverse Event
Injury ·SYNTHES MONUMENT·Product code HWC·October 6, 2008

9800

FDA Adverse Event
Malfunction ·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·June 18, 2013

ALARIS PUMP MODULE

FDA Adverse Event
Malfunction ·CAREFUSION CORP·Product code FRN·June 29, 2011

SOF-FLEX PEDIATRIC DOUBLE PIGTAIL URETERAL STENT SET

FDA Adverse Event
Injury ·COOK INC·Product code FAD·September 30, 2024

SOF-FLEX PEDIATRIC DOUBLE PIGTAIL URETERAL STENT SET

FDA Adverse Event
Injury ·COOK INC·Product code FAD·October 7, 2024

SOF-FLEX MULTI-LENGTH URETERAL STENT SET

FDA Adverse Event
Injury ·COOK INC·Product code FAD·October 21, 2024

SOF-FLEX PEDIATRIC DOUBLE PIGTAIL URETERAL STENT SET

FDA Adverse Event
Injury ·COOK INC·Product code FAD·April 19, 2021

SOF-FLEX PEDIATRIC DOUBLE PIGTAIL URETERAL STENT SET

FDA Adverse Event
Injury ·COOK INC·Product code FAD·April 19, 2021