24 results
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22ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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CAYMAN SCREWS MODEL K2-12-1000-XX, K2-12-1001-XX
FDA 510(k)
FDA Class 2
·Orthopedic
ELMED
FDA UDI
ELMED INCORPORATED·00842180170391·JORDAN-SIMPSON SEGMENTED RING, SLOTTED, LARGE, ...
SAVANNAH-T
FDA UDI
SPINAL ELEMENTS·00840916150006·SAVANNAH®-T ROD TEMPLATE, 5.5MM OD, 200MM L
PerformancePlus™
FDA UDI
GRAPHIC CONTROLS ACQUISITION CORP·10813150021019·
ClearScan™
FDA UDI
GRAPHIC CONTROLS ACQUISITION CORP·40813150020495·Radiolucent Electrodes
60 PER POUCH, 10 POUCHE...
NIDO Pedicle Screw System
FDA UDI
Kalitec Direct LLC·B07315K0100610·Caddie Lid, Modular Bone Screws
BIPAP A40 PRO
FDA Adverse Event
Malfunction
·RESPIRONICS, INC.·Product code MNT·September 26, 2024
DIMENSION CLINICAL CHEMISTRY SYSTEM, MODEL XPAND
FDA 510(k)
FDA Class 2
·Clinical Chemistry
MINXRAY HF70D HIGH FREQUENCY PORTABLE DENTAL X-RAY UNIT
FDA 510(k)
FDA Class 2
·Dental
NEONATAL BUBBLE CPAP DUAL HEATED CIRCUIT KIT
FDA Adverse Event
Malfunction
·Product code BZE·March 3, 2021
BUBBLE CPAP CIRCUIT
FDA Adverse Event
Malfunction
·FISHER & PAYKEL HEALTHCARE LIMITED·Product code BZD·April 19, 2011
BUBBLE CPAP CIRCUIT
FDA Adverse Event
Malfunction
·FISHER & PAYKEL HEALTHCARE LIMITED·Product code BZD·April 19, 2011
ANIMAS INSULIN INFUSION PUMP
FDA Adverse Event
Malfunction
·ANIMAS CORPORATION·Product code LZG·May 8, 2013
PERFORATOR DRIVER W/HUDSON END
FDA Adverse Event
Malfunction
·DEPUY SYNTHES POWER TOOLS·Product code HBE·September 18, 2014
GYNNIE OB-GYN STRETCHER
FDA Adverse Event
Malfunction
·STRYKER MEDICAL·Product code HDD·May 16, 2011
30K FSI-SLI-1000 INSERT,PKD
FDA Adverse Event
Malfunction
·DENTSPLY LLC·Product code ELC·March 4, 2025
BUBBLE CPAP GENERATOR
FDA Adverse Event
Malfunction
·FISHER & PAYKEL HEALTHCARE LIMITED·Product code BZD·February 16, 2017
BUBBLE CPAP GENERATOR
FDA Adverse Event
Malfunction
·FISHER & PAYKEL HEALTHCARE LTD·Product code BZD·December 22, 2016
BUBBLE CPAP GENERATOR
FDA Adverse Event
Malfunction
·FISHER & PAYKEL HEALTHCARE LIMITED·Product code BZD·February 16, 2017
REFORM PEDICLE SCREW SYSTEM
FDA Adverse Event
Malfunction
·PRECISION SPINE, INC.·Product code HXX·November 11, 2021