301 results · 21ms · 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.

SimplyGo Mini

FDA UDI
Respironics, Inc.·00606959033818·SimplyGo Mini, IKK

SIMPLYGO MINI,STND BATTERY,IKK

FDA Adverse Event
Malfunction ·RESPIRONICS, INC.·Product code CAW·May 7, 2025

SimplyGo Mini

FDA UDI
Respironics, Inc.·00606959033832·SimplyGo Mini with Extended Battery, IKK.

SimplyGo Mini

FDA UDI
Respironics, Inc.·00606959033825·SimplyGo Mini with Standard Battery, IKK.

EverFlo

FDA UDI
Respironics, Inc.·00606959032569·EverFlo w/Oxygen Percentage Indicator, 230V, IKK

LAG SCREW, TI GAMMA3 Ø10.5X90MM

FDA Adverse Event
Injury ·STRYKER TRAUMA KIEL·Product code HSB·June 13, 2013

BODYMEDIA FIT

FDA Adverse Event
Injury ·BODYMEDIA, INC.·Product code IKK·April 15, 2014

LOKOMAT PRO

FDA Adverse Event
Injury ·HOCOMA AG·Product code IKK·November 30, 2017

KIN COM

FDA Adverse Event
Injury ·CHATTANOOGA GROUP, INC.·Product code IKK·March 2, 1994

SYSTEM, ISOKINETIC TESTING AND EVALUATION

FDA Adverse Event
Other ·BIODEX MEDICAL SYSTEMS, INC.·Product code IKK·November 6, 2009

*

FDA Adverse Event
Malfunction ·BIODEX MEDICAL SYSTEMS, INC·Product code IKK·October 6, 2009

KIN-COM 125E

FDA Adverse Event
Injury ·CHATTANOOGA GROUP, INC.·Product code IKK·June 25, 1999

KIN-COM 125 A/P

FDA Adverse Event
Injury ·CHATTANOOGA GROUP, INC.·Product code IKK·April 19, 1999

ECCENTRON

FDA Adverse Event
Other ·BTE TECHNOLOGIES, INC.·Product code IKK·February 27, 2014

CYBEX NORM ISOKINETIC UNIT

FDA Adverse Event
Other ·CYBEX·Product code IKK·July 25, 1997

ER

FDA Adverse Event
Other ·BTE TECHNOLOGIES, INC.·Product code IKK·April 19, 2013

CYBEX NORM ISOKINETIC UNIT

FDA Adverse Event
Injury ·CYBEX·Product code IKK·May 28, 1997

KIN-COM II

FDA Adverse Event
Other ·CHATTANOOGA GROUP, INC.·Product code IKK·September 25, 1998

LOKOMATPRO

FDA Adverse Event
Injury ·HOCOMA AG·Product code IKK·May 20, 2022

SYSTEM, ISOKINETIC TESTING AND EVALUATION

FDA Adverse Event
Malfunction ·Product code IKK·June 10, 2022