17 results · 30ms · Sources: EU EUDAMED, US FDA

Get notified when this changes

We'll email you when new records match this search — new devices, new clearances, certificate changes, or withdrawals.

Xia® Growth Rod Conversion Set

FDA 510(k)
FDA Class 2 ·Orthopedic

MEDI

FDA UDI
MEDI MANUFACTURING, INC.·04051526550131·GENUMEDI PT KNEE SUP SILVER L EW IV

OsteoMed

FDA UDI
OSTEOMED LLC·00845694009034·2 x 4 Hole Compression Left L Plate

LACTOSORB* 2.0MM SYSTEM TEMPLATE

FDA UDI
BIOMET MICROFIXATION, INC·00841036053840·

SELMAN TISSUE FORCEPS

FDA UDI
SONTEC INSTRUMENTS, INC.·00192896024069·SELMAN TISSUE FORCEPS ROUND CUP TEETH

MDL SERIES DIODE LASERS, MODEL MDL-10/15

FDA 510(k)
FDA Class 2 ·General, Plastic Surgery

MEDRANGE ELECTROSURGICAL GENERATOR

FDA 510(k)
FDA Class 2 ·General, Plastic Surgery

FASTTAKE

FDA Adverse Event
Malfunction ·LIFESCAN, INC.·Product code CFR·September 26, 2002

ACCU-CHEK COMFORT CURVE TEST STRIPS

FDA Adverse Event
Malfunction ·ROCHE DIAGNOSTICS·Product code LFR·September 7, 2007

ASPEN FLEXIBLE LIGHT HANDLE COVER, STERILE

FDA Adverse Event
Malfunction ·ASPEN SURGICAL PRODUCTS, CALEDONIA·Product code FTA·October 30, 2018

SYRINGE 5ML SALINE FILL CHINA SP

FDA Adverse Event
Malfunction ·BECTON DICKINSON·Product code NGT·June 25, 2025

PARADIGM REAL-TIME INSULIN INFUSION PUMP

FDA Adverse Event
Malfunction ·MEDTRONIC MINIMED·Product code OYC·October 4, 2014

BHR

FDA Adverse Event
Injury ·SMITH & NEPHEW ORTHOPAEDICS LTD·Product code NXT·June 3, 2013

EON IMPLANTABLE PULSE GENERATOR

FDA Adverse Event
Malfunction ·ST. JUDE MEDICAL - NEUROMODULATION·Product code LGW·May 25, 2011

ESOPHYX Z

FDA Adverse Event
Injury ·ENDOGASTRIC SOLUTIONS, INC.·Product code ODE·June 22, 2017

EVERSENSE E3 SENSOR

FDA Adverse Event
Malfunction ·SENSEONICS INC.·Product code QHJ·November 20, 2025

TRUE METRIX

FDA Adverse Event
Malfunction ·TRIVIDIA HEALTH INC·Product code NBW·July 18, 2024