27 results
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28ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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PERMADYNE POLYETHER RUBBER IMPRESSION
FDA 510(k)
FDA Class 2
·Dental
VITROS
FDA UDI
ORTHO CLINICAL DIAGNOSTICS·10758750000517·VITROS Immunodiagnostic Products NTx Calibrators
Trimline
FDA UDI
ORMCO CORPORATION·00889989051353·UPPER LEFT FIRST MOLAR TRIMLINE BAND SIZE 31
ORTHO ARCH
FDA UDI
Ortho Arch Company Inc·D9098000311·ANTERIOR BRACKET PLACER
Rampart O
FDA UDI
SPINEOLOGY INC.·M7402800031·7x40mm Trial
MTS Knee
FDA UDI
MEDTRONIC, INC.·00643169778276·TRAY 90-SRK-800031 FEMORAL TRIAL CR/CS
Responsive Orthopedics Total Knee Arthroplasty System
FDA UDI
RESPONSIVE ORTHOPEDICS, LLC·00841973108443·Femoral Trials - CR/CS Case
TASMIN R
FDA UDI
SIGNUS Medizintechnik GmbH·04047844050019·An orthopedic manual surgical instrument is a n...
TASMIN R
FDA UDI
SIGNUS Medizintechnik GmbH·04047844050033·An orthopedic manual surgical instrument is a n...
Lenses, Soft Contact, Daily Wear
FDA Pre-Market Approval
FDA Class 2
·(MAFILCON) SOFT CONTACT LENSES
AQUANET, MODEL EC 2000
FDA 510(k)
FDA Class 2
·Gastroenterology, Urology
IND ONE STEP FECAL OCCULT BLOOD TEST MODEL 440-10
FDA 510(k)
FDA Class 2
·Hematology
SYRINGE 50ML LL TIP 1ML
FDA Adverse Event
Malfunction
·BECTON DICKINSON·Product code FMF·February 7, 2024
SPECTRUM INFUSION PUMP
FDA Adverse Event
Malfunction
·BAXTER HEALTHCARE CORPORATION·Product code FRN·January 8, 2014
6800
FDA Adverse Event
Malfunction
·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·October 17, 2012
9600
FDA Adverse Event
Malfunction
·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·August 11, 2010
AIRSEAL
FDA Adverse Event
Malfunction
·CONMED·Product code HIF·December 17, 2025
AIRSEAL IFS, 110V
FDA Adverse Event
Injury
·W.O.M. WORLD OF MEDICINE GMBH·Product code HIF·October 20, 2020
AIRSEAL IFS, 110V
FDA Adverse Event
Injury
·W.O.M. WORLD OF MEDICINE GMBH·Product code HIF·August 23, 2023
AIRSEAL IFS, 110V
FDA Adverse Event
Malfunction
·W.O.M. WORLD OF MEDICINE GMBH·Product code HIF·June 19, 2024