15 results · 36ms · Sources: EU EUDAMED, US FDA

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NuVasive(r) Monolith Corpectomy System

FDA 510(k)
FDA Class 2 ·Orthopedic

Walgreens

FDA UDI
WALGREEN CO.·00049022632899·MAXIPAD OVERNIGHT UNSCENTED 28CNT

SCREW, BONE, 4 MM OD X 5.0 (127 MM) IN LG, STRIDE

FDA Adverse Event
Malfunction ·BLUE BELT TECHNOLOGIES·Product code OLO·April 23, 2020

SCREW, BONE, 4 MM OD X 5.0 (127 MM) IN LG, STRIDE

FDA Adverse Event
Malfunction ·BLUE BELT TECHNOLOGIES·Product code OLO·April 23, 2020

SCREW, BONE, 4 MM OD X 5.0 (127 MM) IN LG, STRIDE

FDA Adverse Event
Malfunction ·BLUE BELT TECHNOLOGIES·Product code OLO·April 23, 2020

VARI AX DISTAL RADIUS LINE EXTENSIONS OF XXL PLATES

FDA 510(k)
FDA Class 2 ·Orthopedic

MAESTRO WRIST PLATING SYSTEM

FDA 510(k)
FDA Class 2 ·Orthopedic

T:SLIM X2 INSULIN PUMP WITH CONTROL-IQ TECHNOLOGY

FDA Adverse Event
Malfunction ·TANDEM DIABETES CARE·Product code QFG·June 27, 2023

T:SLIM X2 INSULIN PUMP WITH CONTROL-IQ TECHNOLOGY

FDA Adverse Event
Malfunction ·TANDEM DIABETES CARE·Product code QFG·November 2, 2023

LEVEL 1 FLUID WARMER IV SET

FDA Adverse Event
Malfunction ·SMITHS HEALTHCARE MANUFACTURING S.A. DE C.V.·Product code KZL·July 15, 2025

ITREL 3

FDA Adverse Event
Malfunction ·MEDTRONIC MED REL MEDTRONIC PUERTO RICO·Product code LGW·June 14, 2013

ALTRUA

FDA Adverse Event
Injury ·GUIDANT CRM CLONMEL IRELAND·Product code NVZ·July 20, 2011

TDXFLX VANCOMYCIN REAGENT

FDA Adverse Event
Malfunction ·ABBOTT DIAGNOSTICS INT'L, LTD·Product code LEH·September 24, 2008

LEVEL 1 FLUID WARMER IV SET

FDA Adverse Event
Malfunction ·ST PAUL·Product code KZL·August 23, 2023

Exactech Equinoxe Constrained Humeral Liner: Item Numbers: a) 320-40-10, b) 320-40-13, Shoulder Arthroplasty

FDA Enforcement
Class II ·Ongoing·Exactech, Inc.·April 10, 2024