26 results
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21ms
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Sources: EU EUDAMED, US FDA
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Regulation: Us FDA
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KURZ UPPER EYELID IMPLANT- PLATINUM/IRIDIUM,MODELS REGULAR 4007 003-007, SPECIAL 4007 002, 4007 008-010
FDA 510(k)
FDA Class 2
·Ophthalmic
Henry Schein
FDA UDI
HENRY SCHEIN, INC.·00304040013830·Zirlux 16+ B1 98.5X18
MSI Precision Specialty Instruments
FDA UDI
Med Saver, Inc.·00194613072018·Tissue Forceps, 1 x 2 Teeth, Overall Length 4-1...
MSI Precision Specialty Instruments
FDA UDI
Med Saver, Inc.·00194613061760·Splinter Forceps, Curved, Without Pin, Overall ...
AMREX-ZETRON, INC.
FDA registration
AMREX-ZETRON, INC.·9 products·🇺🇸 United States
Zavation
FDA UDI
Zavation LLC·00197157009854·11.5mm TAP, CANNULATED
MATIRA ANTERIOR CERVICAL SYSTEM
FDA UDI
Kalitec Direct LLC·B07307K0111101·AWL, 10MM SPRING LOADED
NIDO Pedicle Screw System
FDA UDI
Kalitec Direct LLC·B07315K0131150·Rocker, Hinged Locking
INSET 30
FDA Adverse Event
Injury
·UNOMEDICAL DEVICES S.A. DE C.V.·Product code FPA·September 17, 2025
INSET 30
FDA Adverse Event
Injury
·UNOMEDICAL DEVICES S.A. DE C.V.·Product code FPA·September 17, 2025
REFLEX ANTERIOR CERVICAL PLATE SYSTEM
FDA 510(k)
FDA Class 2
·Orthopedic
ULTRA CATHETER SET
FDA 510(k)
FDA Class 2
·Obstetrics/Gynecology
AUTOSOFT 30
FDA Adverse Event
Malfunction
·UNOMEDICAL DEVICES S.A. DE C.V.·Product code FPA·July 23, 2025
SOLETRA
FDA Adverse Event
Malfunction
·MEDTRONIC NEUROMODULATION·Product code MHY·December 19, 2011
TT MB BASEPLATE
FDA Adverse Event
Injury
·LIMACORPORATE S.P.A·Product code KWT·January 26, 2026
NATURALYTE
FDA Adverse Event
Injury
·FRESENIUS MEDICAL CARE NORTH AMERICA·Product code KPO·March 15, 2013
OT PING METER
FDA Adverse Event
Malfunction
·LIFESCAN INC.·Product code NBW·March 8, 2011
ISOFLEX S
FDA Adverse Event
Injury
·ST JUDE MEDICAL CARDIAC RHYTHM MANAGEMENT DIVISION·Product code DTB·March 10, 2008
ACTIVA
FDA Adverse Event
Injury
·MEDTRONIC NEUROMODULATION·Product code MHY·December 20, 2011
REGEN/RNGLC+ SOLID 62MM SZ 25
FDA Adverse Event
Injury
·ZIMMER BIOMET, INC.·Product code LPH·April 9, 2018