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

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Ventilator, Non-continuous (Respirator)

FDA 510(k)
FDA Class 2 ·Anesthesiology

Dornier MedTech

FDA UDI
Dornier MedTech GmbH·04049958002113·550 Micron 5X Reusable Lightguide, 150 watt, ba...

24M - Tampa Electric Co.

FDA UDI
Certified Safety Manufacturing, Inc.·00766588013497·24M Tampa Electric Co.

Puget Sound Energy - 18 Metal

FDA UDI
Certified Safety Manufacturing, Inc.·00766588014692·Puget Sound Energy - 18 Metal

Ionto Plus Butterfly 2.0 cc

FDA UDI
COMPASS HEALTH BRANDS CORP.·00853904006001·Iontophoresis Drug Delivery Electrodes

MODEL R1000 IR INSULIN PUMP, EZLINK SOFTWARE, SERMON SOFTWARE, R1000 IR DOWNLOAD CRADLE, AND SERIAL INTERFACE ADAPTOR DO

FDA 510(k)
FDA Class 2 ·General Hospital

ORTHOCEPH OC100 D

FDA 510(k)
FDA Class 2 ·Dental

ACUTWIST

FDA Adverse Event
Malfunction ·ACUMED LLC·Product code HWC·January 22, 2019

ACUTWIST

FDA Adverse Event
Malfunction ·ACUMED LLC·Product code HWC·January 22, 2019

ACUTWIST

FDA Adverse Event
Malfunction ·ACUMED LLC·Product code HWC·January 22, 2019

DEXCOM G7 CONTINUOUS GLUCOSE MONITORING SYSTEM

FDA Adverse Event
Malfunction ·DEXCOM, INC.·Product code QBJ·July 29, 2025

ACUTWIST

FDA Adverse Event
Malfunction ·ACUMED LLC·Product code HWC·January 22, 2019

SWANSON FINGER JOINT

FDA Adverse Event
Injury ·WRIGHT MEDICAL TECHNOLOGY, INC.·Product code KWF·December 27, 2018

OT VERIO IQ METER

FDA Adverse Event
Injury ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·October 27, 2014

ACUVUE 2 BRAND CONTACT LENSES

FDA Adverse Event
Injury ·VISTAKON·Product code LPL·June 28, 2013

COOL PATH 7F, 1304-CP-7-25-L-AB (USA)

FDA Adverse Event
Malfunction ·ST. JUDE MEDICAL - IRVINE·Product code OAD·August 3, 2011

INTEGRITY RX

FDA Adverse Event
Injury ·MEDTRONIC IRELAND·Product code MAF·December 23, 2015

INTEGRITY RX

FDA Adverse Event
Injury ·MEDTRONIC IRELAND·Product code MAF·July 28, 2016

SYNCHROMED II

FDA Adverse Event
Injury ·MEDTRONIC NEUROMODULATION·Product code LKK·October 1, 2014

SYNCHROMED II

FDA Adverse Event
Injury ·MEDTRONIC NEUROMODULATION·Product code LKK·October 1, 2014