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

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AUDIOSCREENER OAE

FDA 510(k)
FDA Class 2 ·Ear, Nose, Throat

EQUATE

FDA UDI
WAL-MART STORES, INC.·00078742082868·THIN LINERS REGULAR UNSCENTED 120 CT

Indeflator

FDA UDI
ABBOTT VASCULAR INC.·08717648013591·20/30 INDEFLATOR Inflation Device 30 atm 20 cc

Henry Schein

FDA UDI
HENRY SCHEIN, INC.·10304040054397·Polycarbonate Crowns

truFreeze

FDA UDI
US Endoscopy·00724995199333·Rapid AV Active Venting Cathether is used with ...

truFreeze

FDA UDI
Csa Medical, Inc.·10857068006102·Rapid AV Catheter, box of 5

truFreeze

FDA UDI
Csa Medical, Inc.·00857068006105·Rapid AV Catheter

AIM 100

FDA UDI
Burton Medical, LLC·00858480006049·FLOOR BASE ASSEMBLY

AIM 100

FDA UDI
Burton Medical, LLC·00858480006247·FLOOR BASE ASSEMBLY

RS-4M+MUSCLE STIMULATOR

FDA 510(k)
FDA Class 2 ·Physical Medicine

ENRAF-NONIUS SONOPULS 190 SYSTEM

FDA 510(k)
FDA Class 2 ·Physical Medicine

BALL HEADS: COCR BALL HEAD 12/14 36 SIZE M 0

FDA Adverse Event
Injury ·MEDACTA INTERNATIONAL SA·Product code JDI·October 20, 2020

20/30 PRIORITY PACK INDEFLATOR

FDA Adverse Event
Malfunction ·ABBOTT VASCULAR·Product code MAV·July 20, 2021

GREENFIELD¿

FDA Adverse Event
Malfunction ·BOSTON SCIENTIFIC - CORK·Product code DTK·March 12, 2013

SM204 M-SERIES W/BIG WHEEL

FDA Adverse Event
Malfunction ·STRYKER MEDICAL·Product code FPO·February 3, 2011

THIN WALLED GORE-TEX STRETCH VASCULAR GRAFT

FDA Adverse Event
Injury ·W.L. GORE & ASSOCIATES, INC.·Product code DSY·February 19, 2008

20/30 PRIORITY PACK INDEFLATOR

FDA Adverse Event
Malfunction ·ABBOTT VASCULAR·Product code MAV·April 20, 2021

20/30 INDEFLATOR -REF 1000184 WPL2122268-01 (2019-03-01)

FDA Recall
Open, Classified ·Abbott Vascular·Product code MAV·March 11, 2022

PEARL EDGE BELL CUP

FDA Adverse Event
Injury ·COOPERSURGICAL, INC.·Product code HDB·August 22, 2024

20/30 PRIORITY PACK INDEFLATOR

FDA Adverse Event
Malfunction ·ABBOTT VASCULAR·Product code MAV·July 20, 2021