23 results · 25ms · Sources: EU EUDAMED, US FDA

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Ellipse Ydun

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

MEDI

FDA UDI
MEDI MANUFACTURING, INC.·04051526768505·GENUMEDI PSS GREEN VI

RESTORIS

FDA UDI
MAKO SURGICAL CORP.·00848486000448·MCK Patellofemoral Component

FUKUSHIMA SUCTION TUBE

FDA UDI
SONTEC INSTRUMENTS, INC.·B0991804060·FUKUSHIMA SUCTION TUBE

Cannula, Suction, acc. Bugge 20cm Ø6mm mini

FDA UDI
Geister Medizintechnik GmbH·04057034040256·Cannula, Suction, acc. Bugge 20cm Ø...

FUKUSHIMA SUCTION TUBE

FDA UDI
SONTEC INSTRUMENTS, INC.·00192896000032·FUKUSHIMA SUCTION TUBE

N/A

FDA UDI
Ortho Development Corporation·00822409128945·4-in-1 Cut Guide w/ Anterior Lip Size 6

Fixed Handle IM Rod

FDA UDI
SIGNATURE ORTHOPAEDICS PTY LTD·09348215063689·

MCK PATELLOFEMORAL- L- SZ 6

FDA Adverse Event
Malfunction ·MAKO SURGICAL CORP.·Product code NPJ·May 26, 2015

FORA V20 BLOOD GLUCOSE MONITORING SYSTEM

FDA 510(k)
FDA Class 2 ·Clinical Chemistry

IPULSE, MODEL I400

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

MCK PATELLOFEMORAL- L- SZ 6

FDA Adverse Event
Malfunction ·MAKO SURGICAL CORP.·Product code NPJ·May 26, 2015

RD SET YI

FDA Adverse Event
Malfunction ·MASIMO - 52 DISCOVERY·Product code DQA·March 29, 2021

RD SET DCI

FDA Adverse Event
Malfunction ·MASIMO - 15750 ALTON PKWY·Product code DQA·February 10, 2023

GMK-SPHERE TIBIAL INSERT FIXED SPHERE FLEX SIZE 4/10 MM R

FDA Adverse Event
Injury ·MEDACTA INTERNATIONAL SA·Product code JWH·July 21, 2020

BELLAVISTA

FDA Adverse Event
Injury ·IMTMEDICAL AG·Product code CBK·March 11, 2021

BLADELESS VP 8MM ST W/ FIXATION

FDA Adverse Event
COVIDIEN·Product code GCJ·October 17, 2014

SOLYX SIS SYSTEM

FDA Adverse Event
Injury ·BOSTON SCIENTIFIC - MARLBOROUGH·Product code FTL·June 20, 2013

COLLEAGUE PRE P1.7

FDA Adverse Event
Malfunction ·BAXTER HEALTHCARE - SINGAPORE·Product code FRN·July 27, 2011

KING LAD SILI CONE SINGLE USE, King Systems, 10 devices/case, ETO Sterile Size 5 / Adult Silicone King LAD¿ Patient Size: >70kg Product Usage: Laryngeal airway

FDA Enforcement
Class II ·Terminated·King Systems Corp.·November 28, 2012