29 results
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27ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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Elecsys Syphilis
FDA 510(k)
FDA Class 2
·Microbiology
CoRoent
FDA UDI
Nuvasive, Inc.·00887517629029·CoRoent Ant TLIF Ti, 11x11x30mm 12°
Luna
FDA UDI
ULTRADENT PRODUCTS, INC.·00883205003171·Luna Opal R Mini .018 UR1 (+12°T +5°A)
Comprehensive SRS
FDA UDI
Biomet Orthopedics, LLC·00880304714786·
LEONE SPA
FDA UDI
LEONE SPA·08033707038887·DB BRACKETS 22 20VS BH CUS U/R L/L
PMT® Halo Systems
FDA UDI
PMT CORPORATION·00650551135838·HALO, 1203-5 VEST X-LARGE, ACRYLIC LINER, 1211-...
Innomed, Inc.
FDA UDI
INNOMED, INC.·00840277104793·Roberts Pin Bender Medium
TX1 TISSUE REMOCAL SYSTEM - MICROTIP
FDA Adverse Event
Malfunction
·AOI, INC.·Product code LFL·January 23, 2014
MYLABSEVEN, MYLABALPHA
FDA 510(k)
FDA Class 2
·Radiology
RANDOX DIGOXIN
FDA 510(k)
FDA Class 2
·Clinical Toxicology
TX1 TISSUE REMOVAL SYSTEM - MICROTIP
FDA Adverse Event
Malfunction
·AMERICAN OPTISURGICAL, INC.·Product code LFL·January 27, 2014
BEBACK CROSSING CATHETER
FDA Adverse Event
Malfunction
·BENTLEY INNOMED GMBH·Product code PDU·December 23, 2025
DEXCOM G7 CONTINUOUS GLUCOSE MONITORING SYSTEM
FDA Adverse Event
Malfunction
·DEXCOM, INC.·Product code QBJ·August 22, 2024
BEBACK CROSSING CATHETER
FDA Adverse Event
Malfunction
·BENTLEY INNOMED GMBH·Product code PDU·November 21, 2025
BEBACK CROSSING CATHETER
FDA Adverse Event
Malfunction
·BENTLEY INNOMED GMBH·Product code PDU·April 30, 2025
BEBACK CROSSING CATHETER
FDA Adverse Event
Malfunction
·BENTLEY INNOMED GMBH·Product code PDU·March 6, 2025
PORTABLE OXYGEN GENERATOR (CONCENTRATOR, HOMEFILL)
FDA Adverse Event
Malfunction
·INVACARE FLORIDA OPERATIONS·Product code CAW·October 29, 2014
ENDOTAK RELIANCE
FDA Adverse Event
Injury
·CPI - DEL CARIBE·Product code NVY·July 8, 2013
ENDOTAK RELIANCE
FDA Adverse Event
Malfunction
·CPI - DEL CARIBE·Product code NVY·November 9, 2015
1628664-2017-00093
FDA Adverse Event
Malfunction
·April 5, 2017