14 results · 19ms · 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.

COLONOSCOPE, 2-CHANNEL LOG (ACMI TX-92)

FDA 510(k)
FDA Class 2 ·Gastroenterology, Urology

Ophthalmic Cannula

FDA UDI
KATENA PRODUCTS, INC.·00841668110621·COAXIAL VISCOELASTIC ASPIRAT-IRRIGAT TIP

Ophthalmic Cannula

FDA UDI
KATENA PRODUCTS, INC.·00841668110652·COAXIAL IRR-ASP TIP 45 DEG W/ SILICONE

Bone Conduction Hearing Aid (G41157, G41158, G41159, G41160, G42151, G42152, G42153, G42154, G42155, G42156, G42157, G42158, G42159, G42160, G43151, G43152, G43153, G43154, G43155, G43156, G45151, G45152, G45153, G45154, G45155, G45156, G45157, G45158, G45159, G45160, G46151, G46152, G46153, G46154, G46155, G46156, G46157, G46158)

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

ACCUWELL 17-ALPHA-HYDROXYPROESTERONE ENZYME IMMUNOASSAY WITH MODELS 6015XX-ECAH

FDA 510(k)
FDA Class 1 ·Clinical Chemistry

PLATE CHOCOLATE II AGAR 100 EA

FDA Adverse Event
Malfunction ·BECTON DICKINSON·Product code JSG·November 1, 2021

PLATE CHOCOLATE II AGAR 100 EA

FDA Adverse Event
Malfunction ·BECTON DICKINSON·Product code JSG·August 11, 2021

PLATE CHOCOLATE II AGAR 100 EA

FDA Adverse Event
Malfunction ·BECTON DICKINSON·Product code JSG·August 25, 2021

ONETOUCHPING GLUCOSEMGMTSYSTEM

FDA Adverse Event
Malfunction ·ANIMAS CORPORATION·Product code LZG·April 21, 2014

TENSION FREE VAGINAL TAPE

FDA Adverse Event
Injury ·ETHICON, INC.·Product code FTL·September 26, 2012

NRG KNEE P/S NRG BEARING INSERT S

FDA Adverse Event
Injury ·STRYKER ORTHOPAEDICS CORK·Product code JWH·July 13, 2010

PLATE CHOCOLATE II AGAR 100 EA

FDA Adverse Event
Malfunction ·BECTON, DICKINSON & CO. (SPARKS)·Product code JSG·May 27, 2022

PLATE CHOCOLATE II AGAR 100 EA

FDA Adverse Event
Malfunction ·BECTON DICKINSON·Product code JSG·August 17, 2021

GE Healthcare, Compact Airway Modules E-CO, E-COV, E-COVX, E-CAiO, E-CAiOV and E-CAiOVX. The Datex-Ohmeda S/5MT Compact Airway Module, E-CAiOVX family is used for monitoring hospital patients respiration, ventilation, and gas exchange status.

FDA Enforcement
Class II ·Terminated·GE Healthcare, LLC·June 25, 2014