12 results
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21ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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Xpert® SA Nasal Complete
FDA 510(k)
FDA Class 2
·Microbiology
SpheRx
FDA UDI
Nuvasive, Inc.·00887517445605·SpheRx®II Conn, 70-85mm, Arch Adj. Trans
Oph. Cystotomes
FDA UDI
KATENA PRODUCTS, INC.·00841668113714·CYSTOTOME REVERSED FORM 25GA
TAPERLOC COMPLETE RASP/PROVISIONAL
FDA UDI
Biomet Orthopedics, LLC·00880304632363·
BONESCALPEL® BONESHAVER, MICROHOOK
FDA Adverse Event
Malfunction
·MISONIX, INC.·Product code LFL·January 31, 2025
LIQUID STABLE HBA1C CONTROL
FDA 510(k)
FDA Class 1
·Clinical Chemistry
Disposable Safety Self-destructive Syringes, 5 ML
FDA 510(k)
FDA Class 2
·General Hospital
TOTAL ASR FEM IMPLANT SZ 55
FDA Adverse Event
Injury
·DEPUY INTERNATIONAL, LTD·Product code KWY·November 21, 2008
DURATA STS OPTIM ACTIVE FIXATION, DF-4 CONNECTOR
FDA Adverse Event
Injury
·ST JUDE MEDICAL CARDIAC RHYTHM MANAGEMENT DIVISION·Product code NVY·September 11, 2011
AJUST ADJUSTABLE SINGLE INCISION SLING
FDA Adverse Event
Malfunction
·BARD SHANNON LIMITED·Product code FTL·July 18, 2013
TECNIS SYNERGY OPTIBLUE IOL
FDA Adverse Event
Injury
·AMO MANUFACTURING NETHERLANDS·Product code POE·September 23, 2021
BONESCALPEL® BONESHAVER, MICROHOOK DISPOSABLE
FDA Adverse Event
Malfunction
·MISONIX, INC.·Product code LFL·November 24, 2024