83 results
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25ms
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Sources: EU EUDAMED, US FDA
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Regulation: Us FDA
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PARCUS 35 KNOTLESS PEEK CF PUSH-IN SUTURE ANCHORS, PARCUS 45 KNOTLESS PEEK CF PUSH-IN SUTURE ANCHORS
FDA 510(k)
FDA Class 2
·Orthopedic
BIO-MODULAR SHOULDER SYSTEM
FDA UDI
Biomet Orthopedics, LLC·00880304213449·
Bio-Modular® Shoulder System
FDA UDI
Biomet Orthopedics, LLC·00887868253546·
Marienfeld Superior
FDA UDI
Paul Marienfeld GmbH & Co. KG·04250317382719·
N/A
FDA UDI
HANS RUDOLPH, INC.·00874750004836·LARG QUEST MASK/HG GRN22OD SWL
Millennium
FDA UDI
Avalign Technologies, Inc.·00190776164898·VEIN RETRACTOR BLADE
BIO-MODULAR SHOULDER SYSTEM
FDA UDI
Biomet Orthopedics, LLC·00880304433687·
ARIEL RADIO FREQUENCY (RF) ELECTROSURGICAL CONTROL MODULE AND ACCESSORIES
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
GE LUNAR VISCERAL FAT SOFTWARE
FDA 510(k)
FDA Class 2
·Radiology
ARCHITECT SYPHILIS TP REAGENT KIT
FDA Adverse Event
Malfunction
·ABBOTT GMBH·Product code LIP·April 8, 2026
ARCHITECT SYPHILIS TP REAGENT KIT
FDA Adverse Event
Malfunction
·ABBOTT GMBH·Product code LIP·May 1, 2026
ALINITY I SYPHILIS TP REAGENT KIT
FDA Adverse Event
Malfunction
·ABBOTT GMBH·Product code LIP·May 4, 2026
ALINITY I SYPHILIS TP REAGENT KIT
FDA Adverse Event
Malfunction
·ABBOTT GMBH·Product code LIP·May 22, 2026
ZEPHIR
FDA Adverse Event
Injury
·MEDTRONIC SOFAMOR DANEK·Product code KWQ·May 15, 2013
HEARTSTREAM FR2
FDA Adverse Event
Malfunction
·PHILIPS MEDICAL SYSTEMS·Product code MKJ·September 17, 2014
SYNCHROMED II
FDA Adverse Event
Injury
·MDT PUERTO RICO OPERATIONS CO., JUNCOS·Product code LKK·June 2, 2011
ALINITY I SYPHILIS TP REAGENT KIT
FDA Adverse Event
Malfunction
·ABBOTT GMBH·Product code LIP·April 13, 2026
ALINITY I SYPHILIS TP REAGENT KIT
FDA Adverse Event
Malfunction
·ABBOTT GMBH·Product code LIP·May 18, 2026
ARCHITECT SYPHILIS TP REAGENT KIT
FDA Adverse Event
Malfunction
·ABBOTT GMBH·Product code LIP·April 22, 2026
ARCHITECT SYPHILIS TP REAGENT KIT
FDA Adverse Event
Malfunction
·ABBOTT GMBH·Product code LIP·May 19, 2026