26 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.

Proton Immobilization Solution

FDA 510(k)
FDA Class 2 ·Radiology

MEDI

FDA UDI
MEDI MANUFACTURING, INC.·04049772813872·GENUMEDI PRO SILVER SIZE VII

POUR-PLUS

FDA UDI
Denplus Inc·D8451151207·POUR-PLUS, MDP, 2.3 kg

Glisten™ Provisional Resin Glaze

FDA UDI
DEN-MAT HOLDINGS, LLC·00359883003814·Provisional Resin Glaze

Glisten™ Provisional Resin Glaze

FDA UDI
CLINICIAN'S CHOICE DENTAL PRODUCTS, INC.·07540172001984·Provisional Resin Glaze

TALOS®-C HA

FDA UDI
MEDITECH SPINE, LLC·B167521512070·

NEODENT IMPLANT SYSTEM

FDA 510(k)
FDA Class 2 ·Dental

CAVEX ORTHOTRACE

FDA 510(k)
FDA Class 2 ·Dental

VACUTRON

FDA UDI
Allied Medical, LLC·00026072007976·CONTINUOUS / INTERMITTENT SUCTION REGULATORS

VITROS CHEMISTRY PRODUCTS GENT REAGENT

FDA Adverse Event
Malfunction ·ORTHO-CLINICAL DIAGNOSTICS·Product code LCD·July 12, 2012

VITROS CHEMISTRY PRODUCTS GENT REAGENT

FDA Adverse Event
Malfunction ·ORTHO-CLINICAL DIAGNOSTICS·Product code LCD·July 12, 2012

VITROS CHEMISTRY PRODUCTS GENT REAGENT

FDA Adverse Event
Malfunction ·ORTHO-CLINICAL DIAGNOSTICS·Product code LCD·July 12, 2012

MINICAP TRANSFER SET

FDA Adverse Event
Malfunction ·BAXTER HEALTHCARE CORPORATION·Product code KDJ·October 6, 2020

VACUTRON

FDA UDI
Allied Medical, LLC·00026072007990·CONTINUOUS / INTERMITTENT SUCTION REGULATORS

VACUTRON

FDA UDI
Allied Medical, LLC·00026072007983·CONTINUOUS / INTERMITTENT SUCTION REGULATORS

VACUTRON

FDA UDI
Allied Medical, LLC·00026072008010·CONTINUOUS / INTERMITTENT SUCTION REGULATORS

VACUTRON

FDA UDI
Allied Medical, LLC·00026072008027·CONTINUOUS / INTERMITTENT SUCTION REGULATORS

VACUTRON

FDA UDI
Allied Medical, LLC·00026072008003·CONTINUOUS / INTERMITTENT SUCTION REGULATORS

MINICAP TRANSFER SET

FDA Adverse Event
Malfunction ·BAXTER HEALTHCARE CORPORATION·Product code KDJ·January 3, 2023

FREESTYLE LITE

FDA Adverse Event
Injury ·Product code NBW·September 14, 2011