27 results · 28ms · Sources: EU EUDAMED, 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