22 results · 24ms · 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.

LIFESTYLES NATURAL PERSONAL LUBRICANT

FDA 510(k)
FDA Class 2 ·Obstetrics/Gynecology

MSI Precision Specialty Instruments

FDA UDI
Med Saver, Inc.·00194613017712·K-Wire, Double Ended, Trocar Point, Diameter Si...

ArgenZ HT+ 98x20 A1-L

FDA UDI
ARGEN CORPORATION, THE·D818122054·Dental porcelain/ceramic restoration kit

Logical PX-Series

FDA UDI
SIGNATURE ORTHOPAEDICS PTY LTD·09348215000394·

V200 VENTILATOR

FDA 510(k)
FDA Class 2 ·Anesthesiology

F 900

FDA 510(k)
FDA Class 2 ·Ophthalmic

V200 / ESPRIT

FDA Adverse Event
Malfunction ·RESPIRONICS CALIFORNIA, LLC·Product code CBK·March 16, 2021

RESPIRONICS

FDA Adverse Event
Malfunction ·RESPIRONICS CALIFORNIA, LLC·Product code CBK·March 28, 2021

GOLDEN COMFORTER

FDA Adverse Event
Malfunction ·GOLDEN TECHNOLOGIES, INC.·Product code INO·October 3, 2012

RESPIRONICS

FDA Adverse Event
Malfunction ·RESPIRONICS CALIFORNIA, LLC·Product code MNT·May 19, 2021

RESPIRONICS

FDA Adverse Event
Malfunction ·RESPIRONICS CALIFORNIA, LLC·Product code CBK·May 20, 2021

RESPIRONICS

FDA Adverse Event
Malfunction ·RESPIRONICS CALIFORNIA, LLC·Product code MNT·June 7, 2021

V200 VENTILATOR

FDA Adverse Event
Malfunction ·RESPIRONICS CALIFORNIA, INC·Product code CBK·December 9, 2020

RESPIRONICS

FDA Adverse Event
Malfunction ·RESPIRONICS CALIFORNIA, LLC·Product code MNT·June 21, 2021

ONETOUCHPING GLUCOSEMGMTSYSTEM

FDA Adverse Event
Malfunction ·ANIMAS CORPORATION·Product code LZG·May 21, 2013

ASR UNI FEMORAL IMPL SIZE 45

FDA Adverse Event
Injury ·DEPUY INTL. LTD.·Product code KWA·June 9, 2011

CONTOUR CURVED CUTTER STAPLER

FDA Adverse Event
Malfunction ·ETHICON ENDO-SURGERY, LLC·Product code GDW·August 14, 2008

SAFESHEATH II 9F

FDA Adverse Event
Malfunction ·OSCOR INC.·Product code DYB·August 10, 2022

SOMATOM Edge Plus-Computed tomography system Model 1026700

FDA Enforcement
Class II ·Ongoing·Siemens Medical Solutions USA, Inc·January 19, 2022

SOMATOM Edge Plus with software syngo.CT VB20 Model #10267000

FDA Enforcement
Class II ·Terminated·Siemens Medical Solutions USA, Inc·December 1, 2021