17 results · 26ms · 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.

CLEARFIL MAJESTY ESTHETIC PLT

FDA 510(k)
FDA Class 2 ·Dental

Paltop

FDA UDI
PALTOP ADVANCED DENTAL SOLUTIONS LTD·07290114691154·Titanium Base Abutment Round, Int. Hex. NP L6mm...

Paltop

FDA UDI
PALTOP ADVANCED DENTAL SOLUTIONS LTD·07290108697971·Guided Countersink Ø3.25mm

INRATIO

FDA Adverse Event
Malfunction ·HEMOSENSE, INC.·Product code JPA·September 14, 2007

RZ Medizintechnik GmbH

FDA UDI
RZ-Medizintechnik GmbH·04049197194495·Tebbet Breast Retractor 70x25m...

INRATIO

FDA Adverse Event
Malfunction ·HEMOSENSE, INC.·Product code JPA·September 28, 2007

WAKO AUTOKIT C4

FDA 510(k)
FDA Class 2 ·Immunology

L.A.M. IPM WOUND GEL

FDA 510(k)
FDA Unclassified ·Unknown

SPECTRA WAVEWRITER

FDA Adverse Event
Injury ·BOSTON SCIENTIFIC NEUROMODULATION CORPORATION·Product code LGW·December 24, 2024

INRATIO

FDA Adverse Event
Malfunction ·HEMOSENSE, INC.·Product code JPA·October 4, 2007

INRATIO

FDA Adverse Event
Malfunction ·HEMOSENSE, INC.·Product code JPA·December 3, 2007

INRATIO

FDA Adverse Event
Malfunction ·HEMOSENSE, INC.·Product code JPA·November 5, 2007

ARROW BALLOON WEDGE CATHETER (X2)

FDA Adverse Event
Malfunction ·TELEFLEX MEDICAL·Product code DYG·March 17, 2013

ATLAS

FDA Adverse Event
Malfunction ·STRYKER MEDICAL·Product code FPO·April 18, 2011

DIMENSION CLINICAL CHEMISTRY SYSTEM

FDA Adverse Event
Malfunction ·SIEMENS HEALTHCARE DIAGONSTICS INC.·Product code JJE·June 27, 2008

PROSTHESIS, KNEE, PATELLO/FEMOROTIBIAL, SEMI-CONSTRAINED, UNCEMENTED, POROUS, CO

FDA Adverse Event
Injury ·SMITH & NEPHEW, INC.·Product code MBH·October 20, 2025

CADD-Solis VIP ambulatory Infusion Pumps, Model 2110. Indicated for the following uses: Intra-arterial, subcutaneous, intraperitoneal, in close proximity to nerves, into an intraoperative site, epidural space or subarachnoid space. Therapies that require a continuous rate of infusion, intermittent bolus, and/or with patient-controlled demand doses.

FDA Enforcement
Class I ·Ongoing·Smiths Medical ASD Inc.·August 14, 2024