17 results
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23ms
·
Sources: EU EUDAMED, US FDA
Ablation Confirmation
FDA 510(k)
FDA Class 2
·Radiology
BRUSIO 2.5mm Reinforced Straight Plate, 22 Hole
FDA UDI
Bonebridge AG·07640187463224·
NA
FDA UDI
KEY SURGICAL, INC.·10849771048746·K-Wires, Double trocar, .035-inch (0.9mm) diame...
KMEDIC
FDA UDI
TELEFLEX INCORPORATED·24026704292374·
mahe medical GmbH
FDA UDI
mahe medical gmbh·04050659483927·K-Wire w. double end trocarpoint _x000D_...
K-Wire w. double end trocarpoint 0.90mm/152mm, 6 pcs./unit
FDA UDI
mahe medical gmbh·EMAHKM710220·K-Wire w. double end trocarpoint
0.90mm...
SCHWERT
FDA UDI
A. Schweickhardt GmbH & Co. KG·E8961710220·Bone spreaders straight 2,2mm
round ...
POWDER-FREE VINYL EXAMINATION GLOVES
FDA 510(k)
FDA Class 1
·General Hospital
PULMOTRACK 5050 WHOLTER, MODEL 5050
FDA 510(k)
FDA Class 2
·Cardiovascular
COOK-SWARTZ DOPPLER PROBE
FDA Adverse Event
Injury
·COOK VANDERGRIFT INC·Product code ITX·May 11, 2022
PORTABLE OXYGEN GENERATOR (CONCENTRATOR, HOMEFILL)
FDA Adverse Event
Malfunction
·INVACARE FLORIDA OPERATIONS·Product code CAW·October 14, 2014
CENTURY STERILIZER
FDA Adverse Event
STERIS MEXICO, S. DE R.L. DE C.V.·Product code FLE·June 14, 2013
GREENLIGHT MOXY
FDA Adverse Event
Malfunction
·AMERICAN MEDICAL SYSTEMS, INNOVATION CENTER - SILICON VALLEY·Product code GEX·June 30, 2011
COOK-SWARTZ DOPPLER PROBE
FDA Adverse Event
Injury
·COOK VANDERGRIFT INC·Product code ITX·November 23, 2022
BD PLASTIPAK¿ HYPODERMIC SYRINGE LUER LOK¿
FDA Adverse Event
Malfunction
·BECTON DICKINSON, S.A.·Product code FMF·March 20, 2018
COOK-SWARTZ DOPPLER PROBE
FDA Adverse Event
Injury
·COOK VANDERGRIFT INC·Product code ITX·August 9, 2023
Philips Ingenia 3.0T with MR Elastography (MRE). 1. Model Number (REF): 781342. 2. Model Number (REF): 781377. 3. Model Number (REF): 782103. 510(k) Numbers: K163116, K173079, K183063, K193215, K213516, K213583, K223458, K251397, K251808
FDA Enforcement
Class II
·Ongoing·Philips North America·May 6, 2026